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非那米柳 | 133-11-9

中文名称
非那米柳
中文别名
对氨基水杨酸苯酯;4-氨基水杨酸苯酯;非那米沙
英文名称
Pheny-PAS-Tebamin
英文别名
phenyl 4-aminosalicylate;fenamisal;phenyl aminosalicylate;phenyl 4-amino-2-hydroxybenzoate
非那米柳化学式
CAS
133-11-9
化学式
C13H11NO3
mdl
MFCD00007788
分子量
229.235
InChiKey
DNVVZWSVACQWJE-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 熔点:
    150-152 °C(lit.)
  • 沸点:
    371.13°C (rough estimate)
  • 密度:
    1.2084 (rough estimate)
  • 溶解度:
    可溶于DMSO(少许)、甲醇(少许)
  • 碰撞截面:
    163.4 Ų [M+H]+ [CCS Type: TW, Method: calibrated with polyalanine and drug standards]

计算性质

  • 辛醇/水分配系数(LogP):
    3.2
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    72.6
  • 氢给体数:
    2
  • 氢受体数:
    4

安全信息

  • 危险品标志:
    Xi
  • 危险类别码:
    R36/37/38
  • WGK Germany:
    3
  • 海关编码:
    2922509090
  • 安全说明:
    S26,S36

SDS

SDS:116d8bd1610aa9cddb38ee835e29eedb
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Name: Phenyl 4-Aminosalicylate 99% Material Safety Data Sheet
Synonym: Phenyl PAS; 4-Amino-2-Hydroxybenzoic Acid Phenyl Ester
CAS: 133-11-9
Section 1 - Chemical Product MSDS Name:Phenyl 4-Aminosalicylate 99% Material Safety Data Sheet
Synonym:Phenyl PAS; 4-Amino-2-Hydroxybenzoic Acid Phenyl Ester

Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS
CAS# Chemical Name content EINECS#
133-11-9 Phenyl 4-Aminosalicylate 99% 205-092-8
Hazard Symbols: XI
Risk Phrases: 36/37/38

Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
Irritating to eyes, respiratory system and skin.
Potential Health Effects
Eye:
Causes eye irritation. May cause chemical conjunctivitis.
Skin:
Causes skin irritation.
Ingestion:
May cause gastrointestinal irritation with nausea, vomiting and diarrhea.
Inhalation:
Causes respiratory tract irritation. Can produce delayed pulmonary edema.
Chronic:
Effects may be delayed.

Section 4 - FIRST AID MEASURES
Eyes: Immediately flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids. Get medical aid immediately.
Skin:
Get medical aid. Flush skin with plenty of water for at least 15 minutes while removing contaminated clothing and shoes. Wash clothing before reuse.
Ingestion:
Never give anything by mouth to an unconscious person. Get medical aid. Do NOT induce vomiting. If conscious and alert, rinse mouth and drink 2-4 cupfuls of milk or water.
Inhalation:
Get medical aid immediately. Remove from exposure and move to fresh air immediately. If breathing is difficult, give oxygen. Do NOT use mouth-to-mouth resuscitation. If breathing has ceased apply artificial respiration using oxygen and a suitable mechanical device such as a bag and a mask.
Notes to Physician:
Treat symptomatically and supportively.

Section 5 - FIRE FIGHTING MEASURES
General Information:
As in any fire, wear a self-contained breathing apparatus in pressure-demand, MSHA/NIOSH (approved or equivalent), and full protective gear. During a fire, irritating and highly toxic gases may be generated by thermal decomposition or combustion. Runoff from fire control or dilution water may cause pollution.
Extinguishing Media:
Use agent most appropriate to extinguish fire. Use water spray, dry chemical, carbon dioxide, or appropriate foam.

Section 6 - ACCIDENTAL RELEASE MEASURES
General Information: Use proper personal protective equipment as indicated in Section 8.
Spills/Leaks:
Vacuum or sweep up material and place into a suitable disposal container. Clean up spills immediately, observing precautions in the Protective Equipment section. Avoid generating dusty conditions.
Provide ventilation.

Section 7 - HANDLING and STORAGE
Handling:
Wash thoroughly after handling. Remove contaminated clothing and wash before reuse. Minimize dust generation and accumulation. Avoid contact with eyes, skin, and clothing. Keep container tightly closed.
Avoid ingestion and inhalation. Use with adequate ventilation.
Storage:
Keep container closed when not in use. Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.

Section 8 - EXPOSURE CONTROLS, PERSONAL PROTECTION
Engineering Controls:
Facilities storing or utilizing this material should be equipped with an eyewash facility and a safety shower. Use adequate ventilation to keep airborne concentrations low.
Exposure Limits CAS# 133-11-9: Personal Protective Equipment Eyes: Wear appropriate protective eyeglasses or chemical safety goggles as described by OSHA's eye and face protection regulations in 29 CFR 1910.133 or European Standard EN166.
Skin:
Wear appropriate protective gloves to prevent skin exposure.
Clothing:
Wear appropriate protective clothing to minimize contact with skin.
Respirators:
Follow the OSHA respirator regulations found in 29 CFR 1910.134 or European Standard EN 149. Use a NIOSH/MSHA or European Standard EN 149 approved respirator if exposure limits are exceeded or if irritation or other symptoms are experienced.

Section 9 - PHYSICAL AND CHEMICAL PROPERTIES

Physical State: Powder
Color: white
Odor: Not available.
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: Not available.
Freezing/Melting Point: 150.00 - 152.00 deg C
Autoignition Temperature: Not applicable.
Flash Point: Not applicable.
Explosion Limits, lower: Not available.
Explosion Limits, upper: Not available.
Decomposition Temperature:
Solubility in water: 0.7mg/100ml
Specific Gravity/Density:
Molecular Formula: C13H11NO3
Molecular Weight: 229.23

Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Stable at room temperature in closed containers under normal storage and handling conditions.
Conditions to Avoid:
Incompatible materials, dust generation, excess heat, strong oxidants.
Incompatibilities with Other Materials:
Acid anhydrides, acid chlorides, acids, chloroformates, oxidizing agents.
Hazardous Decomposition Products:
Nitrogen oxides, carbon monoxide, irritating and toxic fumes and gases, carbon dioxide, nitrogen.
Hazardous Polymerization: Has not been reported

Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 133-11-9 unlisted.
LD50/LC50:
Not available.
Carcinogenicity:
Phenyl 4-Aminosalicylate - Not listed by ACGIH, IARC, or NTP.

Section 12 - ECOLOGICAL INFORMATION


Section 13 - DISPOSAL CONSIDERATIONS
Dispose of in a manner consistent with federal, state, and local regulations.

Section 14 - TRANSPORT INFORMATION

IATA
Not regulated as a hazardous material.
IMO
Not regulated as a hazardous material.
RID/ADR
Not regulated as a hazardous material.

Section 15 - REGULATORY INFORMATION

European/International Regulations
European Labeling in Accordance with EC Directives
Hazard Symbols: XI
Risk Phrases:
R 36/37/38 Irritating to eyes, respiratory system
and skin.
Safety Phrases:
S 24/25 Avoid contact with skin and eyes.
WGK (Water Danger/Protection)
CAS# 133-11-9: No information available.
Canada
None of the chemicals in this product are listed on the DSL/NDSL list.
CAS# 133-11-9 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 133-11-9 is not listed on the TSCA inventory.
It is for research and development use only.


SECTION 16 - ADDITIONAL INFORMATION
N/A

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    非那米柳重水 作用下, 以 四氢呋喃 为溶剂, 80.0 ℃ 、101.33 kPa 条件下, 反应 3.0h, 以84%的产率得到
    参考文献:
    名称:
    NHC 稳定的铱纳米颗粒作为苯胺氢同位素交换反应的催化剂。
    摘要:
    报道了 N-杂环卡宾稳定铱纳米颗粒的制备及其在氢同位素交换反应中的应用。这些空气稳定且易于处理的铱纳米颗粒显示出独特的催化活性,允许使用 D2 或 T2 作为同位素源选择性和高效地将氢同位素掺入苯胺上。这种转化的有用性已经通过各种复杂药物的氘和氚标记得到证明。
    DOI:
    10.1002/anie.201914369
  • 作为产物:
    描述:
    苯酚盐酸溶剂黄146三氯氧磷 作用下, 生成 非那米柳
    参考文献:
    名称:
    Studies on Antituberculotics. I. Preparation of Aryl p-Aminosalicylates
    摘要:
    DOI:
    10.1021/ja01130a037
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文献信息

  • FUNCTIONALLY-MODIFIED OLIGONUCLEOTIDES AND SUBUNITS THEREOF
    申请人:Sarepta Therapeutics, Inc.
    公开号:US20140330006A1
    公开(公告)日:2014-11-06
    Functionally-modified oligonucleotide analogues comprising modified intersubunit linkages and/or modified 3′ and/or 5′-end groups are provided. The disclosed compounds are useful for the treatment of diseases where inhibition of protein expression or correction of aberrant mRNA splice products produces beneficial therapeutic effects.
    提供了包含修改的亚单位间连接和/或修改的3'和/或5'-末端基团的功能修饰寡核苷酸类似物。所公开的化合物对于治疗需要抑制蛋白质表达或纠正异常mRNA剪接产物以产生有益治疗效果的疾病是有用的。
  • [EN] GOLD COMPOUNDS AND THEIR USE IN THERAPY<br/>[FR] COMPOSÉS D'OR ET LEUR UTILISATION DANS LE CADRE D'UNE THÉRAPIE
    申请人:AUSPHERIX LTD
    公开号:WO2018220171A1
    公开(公告)日:2018-12-06
    Compound of formula (I) and pharmaceutically acceptable salts and solvates thereof are described, wherein: Px selected from (P1), (P2) or (P3); The compounds are useful in the prevention or treatment of a bacterial infection.
    描述了化合物的公式(I)及其药用可接受的盐和溶剂化合物,其中:Px选自(P1)、(P2)或(P3);这些化合物在预防或治疗细菌感染方面是有用的。
  • Inhibitors of prenyl-protein transferase
    申请人:Merck & Co., Inc.
    公开号:US06297239B1
    公开(公告)日:2001-10-02
    The present invention is directed to compounds which inhibit a prenyl-protein transferase (FTase) and the farnesylation of the oncogene protein Ras. The invention is further directed to chemotherapeutic compositions containing the compounds of this invention and methods for inhibiting a prenyl-protein transferase and the prenylation of the oncogene protein Ras.
    本发明涉及抑制前脂蛋白转移酶(FTase)和致癌基因蛋白Ras的法尼醇化的化合物。该发明进一步涉及含有本发明化合物的化疗组合物以及抑制前脂蛋白转移酶和致癌基因蛋白Ras的方法。
  • Quinclidine derivatives as squalene synthase inhibitors
    申请人:Zeneca Limited
    公开号:US05691349A1
    公开(公告)日:1997-11-25
    Quinuclidine derivatives of formula, and their pharmaceutically acceptable salts, in which: R.sup.1 is hydrogen or hydroxy; R.sup.2 is hydrogen; pr R.sup.1 and R.sup.2 are joined together so that CR.sup.1 -CR.sup.2 is a double bond; X is selected from --CH.sub.2 CH.sub.2 --, --CH.dbd.CH--, --C.dbd.C--, --CH.sub.2 O--, --OCH.sub.2 --, --CH.sub.2 NH--, NHCH.sub.2 --, --CH.sub.2 CO--, --COCH.sub.2 --, --CH.sub.2 S(O).sub.n -- and --S(O).sub.n CH.sub.2 -- wherein n is 0, 1 or 2; and AR is phenyl which may be optionally unsubstituted or substituted by one or more substituents such as halogeno, hydroxy, amino, nitro, cyano, carboxy, carbamoyl, alkyl, alkenyl, alkynyl, alkoxy, alkylamino, dialkylamino, N-alkylcarbamoyl, N,N-di-alkylcarbamoyl, alkoxycarbonyl, alkythio, alkylsulphinyl, alkylsulphonyl, halogeno alkyl, alkanoylamino, alkylenedioxy, alkanoyl and oxime derivatives thereof and O-alkyl ethers of said oximes; provided that when X is selected from --OCH.sub.2 --, --NHCH.sub.2 --, and SCH.sub.2 --, R.sup.1 is not hydroxy; inhibit squalene synthase and are useful in treating diseases or medical conditions in which inhibition of squalene synthase is desirable. The use of such heterocyclic derivatives in treating conditions such as hypercholesterolemia, and atherosclerosis is referred to as well as novel compounds, processes for their preparation and pharmaceutical compositions containing them.
    喹诺克林衍生物的公式,以及它们的药用可接受盐,其中:R.sup.1是氢或羟基;R.sup.2是氢;或者R.sup.1和R.sup.2连接在一起,使得CR.sup.1-CR.sup.2是一个双键;X选自--CH.sub.2 CH.sub.2 --, --CH.dbd.CH--, --C.dbd.C--, --CH.sub.2 O--, --OCH.sub.2 --, --CH.sub.2 NH--, NHCH.sub.2 --, --CH.sub.2 CO--, --COCH.sub.2 --, --CH.sub.2 S(O).sub.n --和--S(O).sub.n CH.sub.2 --,其中n为0、1或2;AR是苯基,它可以是未取代的,也可以是取代的,取代基可以是卤素、羟基、基、硝基、基、羧基、基甲酰基、烷基、烯基、炔基、烷氧基、烷基基、二烷基基、N-烷基基甲酰基、N,N-二烷基基甲酰基、烷氧基羰基、烷基、烷基亚磺酰基、烷基亚磺酰基、卤代烷基、烷酰基、烷二氧基、烷酰和生物以及所述的O-烷基醚;当X选自--OCH.sub.2 --, --NHCH.sub.2 --和--SCH.sub.2 --时,R.sup.1不是羟基;抑制角鲨烯合酶,在抑制角鲨烯合酶是可取的情况下,用于治疗疾病或医疗状况。此类杂环衍生物在治疗高胆固醇血症和动脉粥样硬化等状况中的应用,以及新的化合物、它们的制备过程和含有它们的药物组合物。
  • Prodrugs containing novel bio-cleavable linkers
    申请人:Satyam Apparao
    公开号:US20060046967A1
    公开(公告)日:2006-03-02
    The invention provides the compounds of formula (I) or pharmaceutically acceptable salts thereof. The invention also provides pharmaceutical compositions comprising one or more compounds of formula I or intermediates thereof and one more of pharmaceutically acceptable carriers, vehicles or diluents. The invention further provides methods of preparation and methods of use of prodrugs including NO-releasing prodrugs, double prodrugs and mutual prodrugs comprising the compounds of formula I.
    本发明提供了公式(I)的化合物或其药用可接受的盐。本发明还提供了包含一个或多个公式I的化合物或其中间体以及一个或多个药用可接受的载体、车辆或稀释剂的药物组合物。本发明进一步提供了包括制备方法和使用方法在内的前药,包括释放一氧化氮的前药、双前药和相互前药,由公式I的化合物组成。
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
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ir
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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同类化合物

非那米柳 雷尼替丁 降钙素(humanreduced),8-L-缬氨酸-(9CI) 间苯甲酰氧基苯乙酮 间苯二甲酸二苯酯 间甲苯基苯甲酸酯 间双没食子酸 醋氨沙洛 邻苯二甲酸苄酯2-乙己基酯 邻苯二甲酸二苯酯-D4 邻苯二甲酸二苯酯 邻甲苯基苯甲酸酯 邻氨基苯甲酸(4-硝基苯基)酯 邻亚苯基二苯甲酸酯 贝诺酯 袋衣酸 血竭黄烷A 萘-1,5-二磺酸-4-[2-(二甲氨基)乙氧基]-2-甲基-5-(丙烷-2-基)苯基2-氨基苯酸酯(1:1) 茶痂衣酸 苯酚,2-[2-[(4-氯苯基)氨基]-4-噻唑基]-,苯酸酯(ester) 苯甲醯柳酸甲酯 苯甲酸苯酯 苯甲酸五氟苯酯 苯甲酸丁香酚酯 苯甲酸4-[[(4-甲氧基苯基)亚甲基]氨基]苯基酯 苯甲酸4-(乙酰氨基)-2-[[2-[4-(乙酰氨基)苯甲酰基]亚肼基]甲基]苯基酯 苯甲酸2-(2-苯并恶唑基)苯酯 苯甲酸-4-甲基苯酯 苯甲酸-(4-环戊基-苯基酯) 苯甲酸-(2-烯丙基-4-溴-苯基酯) 苯甲酸-(2-溴-4,6-二硝基-苯基酯) 苯甲酸-(2,4-二溴-3-甲基-苯基酯) 苯甲酸-(2,4-二氯-5-甲基-苯基酯) 苯甲酸-(2,4-二叔丁基苯基酯) 苯甲酸,4-羟基-,4-[(4-羟基苯氧基)羰基]苯基酯 苯甲酸,4-羟基-,4-(己氧基)苯基酯 苯甲酸,4-羟基-,4-(十四烷氧基)苯基酯 苯甲酸,4-羟基-,4-(十二烷氧基)苯基酯 苯甲酸,4-甲酰基-,4-(辛氧基)苯基酯 苯甲酸,4-甲氧基-,2-甲酰基苯基酯 苯甲酸,4-甲基-,4-甲基苯基酯 苯甲酸,4-戊基-,4-(壬氧基)苯基酯 苯甲酸,4-丁氧基-,1,4-亚苯基酯 苯甲酸,4-[[[3-[(2,2-二甲基-1-羰基丙氧基)甲基]-3,4-二氢-2-甲基-4-羰基-6-喹唑啉基]甲基]-2-炔丙基氨基]-,五氟苯基酯 苯甲酸,4-[1-(己氧基)乙基]-,4-(辛氧基)苯基酯 苯甲酸,4-(辛氧基)-,4-[[4-[[(1-甲基庚基)氧代]羰基]苯基]乙炔基]苯基酯 苯甲酸,4-(苯基甲氧基)-,4-(癸氧基)苯基酯 苯甲酸,4-(苯基甲氧基)-,4-(壬氧基)苯基酯 苯甲酸,4-(苯基甲氧基)-,4-(十二烷氧基)苯基酯 苯甲酸,4-(癸氧基)-,4-[氰基[(1-羰基戊基)氧代]甲基]苯基酯,(R)-