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1-苄基高哌嗪 | 4410-12-2

中文名称
1-苄基高哌嗪
中文别名
1-苄基高哌嗪,98;1-苄基-1,4-二氮杂庚烷;N-苄基高哌嗪;1-苄基-1,4-二氮杂环庚烷;1-苄基高哌嗪,98%;1-苄基-1,4-二氮环庚烷;1-苄基-1,4-二氮杂戊烷;苄基高哌嗪;1-(苯基甲基)-1,4-二氮杂环庚烷
英文名称
1-benzyl-[1,4]diazepane
英文别名
N-benzyl homopiperazine;1-Benzyl-1,4-diazepane
1-苄基高哌嗪化学式
CAS
4410-12-2
化学式
C12H18N2
mdl
MFCD00800858
分子量
190.288
InChiKey
JTJTYCPQUOROFM-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:
    54-56 °C
  • 沸点:
    93 °C
  • 密度:
    1.028 g/mL at 25 °C
  • 闪点:
    >230 °F
  • 稳定性/保质期:
    在常温常压下,该物质是稳定的。

计算性质

  • 辛醇/水分配系数(LogP):
    1.5
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    15.3
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 危险等级:
    8
  • 危险品标志:
    Xn,Xi,C
  • 危险类别码:
    R34
  • 危险品运输编号:
    2735
  • WGK Germany:
    2
  • 海关编码:
    2933990090
  • 包装等级:
    III
  • 危险类别:
    8
  • 安全说明:
    S26,S36
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H335
  • 储存条件:
    避光、存于通风干燥处,并密封保存。

SDS

SDS:4aadc586b18b3e0288d2bb77a31818a7
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Name: 1-Benzyl-1 4-diazepane Material Safety Data Sheet
Synonym: None Known
CAS: 4410-12-2
Section 1 - Chemical Product MSDS Name:1-Benzyl-1 4-diazepane Material Safety Data Sheet
Synonym:None Known

Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS
CAS# Chemical Name content EINECS#
4410-12-2 1-Benzyl-1,4-diazepane 90+ unlisted
Hazard Symbols: C
Risk Phrases: 35

Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
Causes severe burns.
Potential Health Effects
Eye:
Causes severe eye burns.
Skin:
Causes severe burns.
Ingestion:
Causes severe digestive tract burns.
Inhalation:
Causes chemical burns to the respiratory tract.
Chronic:
Chronic exposure may cause effects similar to those of acute exposure.

Section 4 - FIRST AID MEASURES
Eyes: Get medical aid immediately. Do NOT allow victim to rub eyes or keep eyes closed. Extensive irrigation with water is required (at least 30 minutes).
Skin:
In case of contact, immediately flush skin with plenty of water for at least 15 minutes while removing contaminated clothing and shoes.
Get medical aid immediately. Wash clothing before reuse.
Ingestion:
If swallowed, do NOT induce vomiting. Get medical aid immediately.
If victim is fully conscious, give a cupful of water. Never give anything by mouth to an unconscious person.
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.
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.
Extinguishing Media:
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:
Absorb spill with inert material (e.g. vermiculite, sand or earth), then place in suitable container. Avoid runoff into storm sewers and ditches which lead to waterways. Clean up spills immediately, observing precautions in the Protective Equipment section. Provide ventilation.

Section 7 - HANDLING and STORAGE
Handling:
Wash thoroughly after handling. Do not breathe dust, vapor, mist, or gas. Do not get in eyes, on skin, or on clothing. Keep container tightly closed. Do not ingest or inhale. Discard contaminated shoes.
Use only with adequate ventilation.
Storage:
Store in a tightly closed container. Corrosives area. Store under an inert atmosphere.

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# 4410-12-2: 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 prevent skin exposure.
Respirators:
A respiratory protection program that meets OSHA's 29 CFR 1910.134 and ANSI Z88.2 requirements or European Standard EN 149 must be followed whenever workplace conditions warrant respirator use.

Section 9 - PHYSICAL AND CHEMICAL PROPERTIES

Physical State: Liquid
Color: colorless
Odor: slight
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: 93-96 deg C @ 0.2mmHg
Freezing/Melting Point: Not available.
Autoignition Temperature: Not available.
Flash Point: Not available.
Explosion Limits, lower: Not available.
Explosion Limits, upper: Not available.
Decomposition Temperature:
Solubility in water:
Specific Gravity/Density:
Molecular Formula: C12H18N2
Molecular Weight: 190.3

Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Stable at room temperature in closed containers under normal storage and handling conditions.
Conditions to Avoid:
None reported.
Incompatibilities with Other Materials:
Oxidizing agents, acids, acid chlorides.
Hazardous Decomposition Products:
Carbon monoxide, oxides of nitrogen, carbon dioxide.
Hazardous Polymerization: Has not been reported.

Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 4410-12-2 unlisted.
LD50/LC50:
Not available.
Carcinogenicity:
1-Benzyl-1,4-diazepane - Not listed by ACGIH, IARC, or NTP.

Section 12 - ECOLOGICAL INFORMATION
Ecotoxicity:
Fish: Pseudomonas putida:

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

Section 14 - TRANSPORT INFORMATION

IATA
Shipping Name: AMINES, LIQUID, CORROSIVE, N.O.S.
Hazard Class: 8
UN Number: 2735
Packing Group: II
IMO
Shipping Name: AMINES, LIQUID, CORROSIVE, N.O.S.
Hazard Class: 8
UN Number: 2735
Packing Group: II
RID/ADR
Shipping Name: AMINES, LIQUID, CORROSIVE, N.O.S.
Hazard Class: 8
UN Number: 2735
Packing group: II

Section 15 - REGULATORY INFORMATION

European/International Regulations
European Labeling in Accordance with EC Directives
Hazard Symbols: C
Risk Phrases:
R 35 Causes severe burns.
Safety Phrases:
S 6 Keep under nitrogen.
S 23 Do not inhale gas/fumes/vapour/spray.
S 26 In case of contact with eyes, rinse immediately
with plenty of water and seek medical advice.
S 36/37/39 Wear suitable protective clothing, gloves
and eye/face protection.
S 45 In case of accident or if you feel unwell, seek
medical advice immediately (show the label where
possible).
WGK (Water Danger/Protection)
CAS# 4410-12-2: No information available.
Canada
None of the chemicals in this product are listed on the DSL/NDSL list.
CAS# 4410-12-2 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 4410-12-2 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:
    1-苄基高哌嗪 在 O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate 、 N,N-二异丙基乙胺三氟乙酸 作用下, 以 二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 162.5h, 生成 1-(4-benzyl-1,4-diazepan-1-yl)-2-[4-(propan-2-yl)morpholin-3-yl]ethan-1-one
    参考文献:
    名称:
    CXCR4 Receptor Antagonists
    摘要:
    披露了一些对CXCR4受体具有拮抗作用的化合物。
    公开号:
    US20130289020A1
  • 作为产物:
    描述:
    ethyl 4-benzylhomopiperazine-1-carboxylate 在 sodium hydroxide 、 sodium chloride 、 氢溴酸 作用下, 生成 1-苄基高哌嗪
    参考文献:
    名称:
    Saturated heterocyclic carboxamide derivatives
    摘要:
    以下是通用公式(I)的饱和杂环羧酰胺衍生物及其盐,具有血小板活化因子(PAF)拮抗活性。
    公开号:
    US04987132A1
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文献信息

  • NOVEL CURCUMIN DERIVATIVE
    申请人:Sugimoto Hachiro
    公开号:US20110082295A1
    公开(公告)日:2011-04-07
    To develop a highly safe measure to treat Alzheimer's disease using a secretase-inhibiting substance, there is provided a compound represented by the following general formula (I) or a salt thereof: wherein A represents a phenyl group or the like, R 1 represents a chlorine atom, a bromine atom, or a nitro group or the like, R 2 , R 3 , R 4 , and R 5 each represent a hydrogen atom or the like, and L represents CH 2 —CH 2 or CH═CH.
    为了开发一种高度安全的措施来治疗阿尔茨海默病,提供了一种由以下一般式(I)或其盐表示的化合物: 其中A代表苯基或类似物,R1代表氯原子、溴原子或硝基团等,R2、R3、R4和R5各自代表氢原子或类似物,L代表CH2—CH2或CH═CH。
  • Synthesis and biological evaluation as AChE inhibitors of new indanones and thiaindanones related to donepezil
    作者:Ziad Omran、Thomas Cailly、Elodie Lescot、Jana Sopkova-de Oliveira Santos、Jean-Hugues Agondanou、Vincent Lisowski、Frédéric Fabis、Anne-Marie Godard、Silvia Stiebing、Guillaume Le Flem、Michel Boulouard、François Dauphin、Patrick Dallemagne、Sylvain Rault
    DOI:10.1016/j.ejmech.2005.07.009
    日期:2005.12
    Sixty-four new indanones and thiaindanones related to donepezil were synthesized and evaluated in vitro as potential AChE inhibitors. Among them, 11 derivatives were found to inhibit the enzyme in the submicromolar range; the best compound revealed its inhibitory activity with an IC50 in the same range (0.06 microM) than the reference compound, donepezil (IC50=0.02 microM).
    合成了与多奈哌齐有关的六十四种新的茚满酮和硫丹酮,并在体外评估了其作为潜在的AChE抑制剂。其中,发现了11种衍生物在亚微摩尔范围内抑制该酶。最好的化合物显示出其抑制活性,其IC50与参考化合物多奈哌齐(IC50 = 0.02 microM)处于相同范围(0.06 microM)。
  • Compounds and uses thereof for decreasing activity of hormone-sensitive lipase
    申请人:——
    公开号:US20030166644A1
    公开(公告)日:2003-09-04
    Use of compounds to inhibit hormone-sensitive lipase, pharmaceutical compositions comprising the compounds, methods of treatment employing these compounds and compositions, and novel compounds. The present compounds are inhibitors of hormone-sensitive lipase and may be useful in the treatment and/or prevention of medical disorders where a decreased activity of hormone-sensitive lipase is desirable.
    使用化合物抑制激素敏感性脂肪酶,包括这些化合物的药物组合物,使用这些化合物和组合物的治疗方法,以及新化合物。目前的化合物是激素敏感性脂肪酶的抑制剂,可能在治疗和/或预防需要降低激素敏感性脂肪酶活性的医学疾病中有用。
  • [EN] HISTONE DEMETHYLASE INHIBITORS<br/>[FR] INHIBITEURS D'HISTONES DÉMÉTHYLASES
    申请人:CHRYSALIS INC
    公开号:WO2017143011A1
    公开(公告)日:2017-08-24
    This disclosure relates to compounds that inhibit histone demethylase activity. In particular, the disclosure relates to compounds that inhibit histone lysine demethylase KDM5B, pharmaceutical compositions and methods of use, such as methods of treating cancer using the compounds and pharmaceutical compositions disclosed herein.
    这份披露涉及抑制组蛋白去甲基化酶活性的化合物。具体而言,该披露涉及抑制组蛋白赖氨酸去甲基化酶KDM5B的化合物,以及使用这些化合物和药物组合物的方法,例如使用本文披露的化合物和药物组合物治疗癌症的方法。
  • Aminomethylpyrimidines as allosteric enhancers of the GABAB receptors
    申请人:Malherbe Pari
    公开号:US20050197337A1
    公开(公告)日:2005-09-08
    The present invention relates to compounds of formula whereinX is —S— or —NH—; R 3 /R 4 together with the N-atom to which they are attached form a non aromatic 5, 6 or 7 membered ring, which optionally contains in addition to the N-atom one additional heteroatom selected from the group consisting of O, S and N, and wherein the ring is optionally substituted by hydroxy, lower alkyl, lower alkoxy, —NR 2 , —CONR 2 , —CO-lower alkyl or benzyl; or R 3 /R 4 form together with the N-atom to which they are attached a heterocyclic ring system, containing two or three rings and which optionally contains one or two additional heteroatoms selected from the group consisting of N and O and which has no more than 20 carbon atoms; and R, R 1 , R 2 , and R 5 are as defined herein and to pharmaceutically suitable acid addition salts thereof. It has been found that the compounds of the invention are active on the GABA B receptor and therefore are useful for the treatment of anxiety, depression, epilepsy, schizophrenia, cognitive disorders, spasticity and skeletal muscle rigidity, spinal cord injury, multiple sclerosis, amyotrophic lateral sclerosis, cerebral palsy, neuropathic pain and craving associated with cocaine and nicotine, psychosis, panic disorder, posttraumatic stress disorders and gastro-intestinal disorders.
    本发明涉及具有以下公式的化合物:其中X是-S-或-NH-;R3/R4与它们所连接的N原子一起形成一个非芳香性的5、6或7元环,该环除了N原子外,还可以选择性地包含一个额外的杂原子,该杂原子选自O、S和N的组中,并且环可以选择性地被羟基、低级烷基、低级烷氧基、-NR2、-CONR2、-CO-低级烷基或苄基取代;或者R3/R4与它们所连接的N原子一起形成一个含有两个或三个环的杂环体系,该体系可以选择性地包含一个或两个额外的杂原子,这些杂原子选自N和O的组中,并且含有的碳原子数不超过20个;以及R、R1、R2和R5如本文所述,以及药用适当的酸加成盐。已经发现,本发明的化合物对GABAB受体具有活性,因此可用于治疗焦虑、抑郁、癫痫、精神分裂症、认知障碍、痉挛和骨骼肌僵直、脊髓损伤、多发性硬化症、肌萎缩侧索硬化症、脑瘫、神经性疼痛以及与可卡因和尼古丁相关的渴望、精神疾病、恐慌症、创伤后应激障碍和胃肠功能障碍。
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