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(4-甲基-2-苯基-1,3-噻唑-5-基)甲胺 | 165735-95-5

中文名称
(4-甲基-2-苯基-1,3-噻唑-5-基)甲胺
中文别名
——
英文名称
1-(4-methyl-2-phenyl-1,3-thiazol-5-yl)methanamine
英文别名
(4-methyl-2-phenylthiazole-5-yl)methylamine;(4-methyl-2-phenylthiazol-5-yl)methanamine;(4-Methyl-2-phenyl-1,3-thiazol-5-yl)methanamine
(4-甲基-2-苯基-1,3-噻唑-5-基)甲胺化学式
CAS
165735-95-5
化学式
C11H12N2S
mdl
MFCD05865105
分子量
204.296
InChiKey
SBCPMNJUNGLHNL-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:
    230 °C
  • 沸点:
    369.1±34.0 °C(Predicted)
  • 密度:
    1.176±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.9
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.181
  • 拓扑面积:
    67.2
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 危险品标志:
    C
  • 海关编码:
    2934100090

SDS

SDS:5e41135d9a7f5cb79905e7d39c356fa2
查看
Name: (4-Methyl-2-phenyl-1 3-thiazol-5-yl)methanamine Material Safety Data Sheet
Synonym: None Known
CAS: 165735-95-5
Section 1 - Chemical Product MSDS Name:(4-Methyl-2-phenyl-1 3-thiazol-5-yl)methanamine Material Safety Data Sheet
Synonym:None Known

Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS
CAS# Chemical Name content EINECS#
165735-95-5 (4-Methyl-2-phenyl-1,3-thiazol-5-yl)me 97+ unlisted
Hazard Symbols: C
Risk Phrases: 35

Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
Causes severe burns.Moisture sensitive.
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.
Keep from contact with moist air and steam. Use only with adequate ventilation.
Storage:
Store in a tightly closed container. Corrosives area. Store protected from moisture. 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# 165735-95-5: 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: Oil
Color: yellow
Odor: slight
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: Not available.
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: C11H12N2S
Molecular Weight: 204.30

Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Stable at room temperature in closed containers under normal storage and handling conditions. Moisture sensitive.
Conditions to Avoid:
Moisture.
Incompatibilities with Other Materials:
Oxidizing agents, acids, acid chlorides, moisture.
Hazardous Decomposition Products:
Carbon monoxide, oxides of nitrogen, oxides of sulfur, carbon dioxide.
Hazardous Polymerization: Will not occur.

Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 165735-95-5 unlisted.
LD50/LC50:
Not available.
Carcinogenicity:
(4-Methyl-2-phenyl-1,3-thiazol-5-yl)methanamine - 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 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# 165735-95-5: No information available.
Canada
None of the chemicals in this product are listed on the DSL/NDSL list.
CAS# 165735-95-5 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 165735-95-5 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:
    (4-甲基-2-苯基-1,3-噻唑-5-基)甲胺二氯甲烷甲苯 为溶剂, 生成 (2-(((4-methyl-2-phenylthiazol-5-yl)methyl)amino)-2-oxoethyl)triphenylphosphonium bromide
    参考文献:
    名称:
    作为癌细胞线粒体靶向抑制剂的新型噻唑衍生物的设计、合成和生物学评价
    摘要:
    线粒体是细胞维持必要代谢活动的关键能量生产来源。针对功能失调的线粒体特征一直是线粒体相关疾病研究的热点。对癌性线粒体代谢的研究是肿瘤治疗中持续关注的问题。在此,我们基于我们早期对线粒体靶向剂的研究,着手评估新型 TPP-噻唑衍生物家族的抗癌活性。具体而言,我们设计并合成了一系列 TPP-噻唑衍生物,并通过 MTT 测定显示大多数合成的化合物有效抑制了三种癌细胞系(HeLa、PC3 和 MCF-7)。在结构修改后,我们探索了 SAR 关系并确定了最有希望的化合物R13(IC50 of 5.52 μM) 用于进一步研究。同时,我们进行了 ATP 产生测定以评估所选化合物对 HeLa 细胞能量产生的抑制作用。结果显示测试化合物显着抑制癌细胞的ATP产生。总体而言,我们设计并合成了一系列对癌细胞具有显着细胞毒性并有效抑制线粒体能量产生的化合物。
    DOI:
    10.1016/j.bioorg.2021.105015
  • 作为产物:
    描述:
    4-甲基-2-苯基-1,3-噻唑-5-甲酸乙酯 在 lithium aluminium tetrahydride 、 邻苯二甲酸亚胺三溴化磷 作用下, 以 四氢呋喃二氯甲烷乙腈 为溶剂, 反应 10.0h, 生成 (4-甲基-2-苯基-1,3-噻唑-5-基)甲胺
    参考文献:
    名称:
    作为癌细胞线粒体靶向抑制剂的新型噻唑衍生物的设计、合成和生物学评价
    摘要:
    线粒体是细胞维持必要代谢活动的关键能量生产来源。针对功能失调的线粒体特征一直是线粒体相关疾病研究的热点。对癌性线粒体代谢的研究是肿瘤治疗中持续关注的问题。在此,我们基于我们早期对线粒体靶向剂的研究,着手评估新型 TPP-噻唑衍生物家族的抗癌活性。具体而言,我们设计并合成了一系列 TPP-噻唑衍生物,并通过 MTT 测定显示大多数合成的化合物有效抑制了三种癌细胞系(HeLa、PC3 和 MCF-7)。在结构修改后,我们探索了 SAR 关系并确定了最有希望的化合物R13(IC50 of 5.52 μM) 用于进一步研究。同时,我们进行了 ATP 产生测定以评估所选化合物对 HeLa 细胞能量产生的抑制作用。结果显示测试化合物显着抑制癌细胞的ATP产生。总体而言,我们设计并合成了一系列对癌细胞具有显着细胞毒性并有效抑制线粒体能量产生的化合物。
    DOI:
    10.1016/j.bioorg.2021.105015
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文献信息

  • Substituted bis-amide metalloprotease inhibitors
    申请人:Sucholeiki Irving
    公开号:US20070155739A1
    公开(公告)日:2007-07-05
    This invention relates to substituted bis-amide pyrimidine compounds of Formula (I), which are useful for the treatment of metalloprotease mediated diseases, in particular MMP-13 related diseases.
    这项发明涉及Formula (I)的取代双酰胺嘧啶化合物,这些化合物对于治疗金属蛋白酶介导的疾病,特别是MMP-13相关疾病是有用的。
  • SPIRO COMPOUND AND USE THEREOF
    申请人:Taniguchi Takahiko
    公开号:US20100069351A1
    公开(公告)日:2010-03-18
    The present invention aims to provide a novel SCD inhibitor. The present invention relate to SCD inhibitor comprising A compound represented by the formula (I) wherein R is an optionally substituted cyclic group or an optionally substituted carbamoyl group, provided that R is not an optionally substituted 7-pyrido[2,3-d]pyrimidyl group; ring A is an optionally further substituted pyridazine ring; R 1 , R 2 , R 3 , R 4 , R 11 , R 12 , R 13 and R 14 are each independently a hydrogen atom or a substituent, or R 1 and R 11 in combination, R 2 and R 12 in combination, R 3 and R 13 in combination, or R 4 and R 14 in combination optionally form an oxo group, or R 2 and R 4 in combination optionally form a bond or an alkylene cross-linkage; m and n are each independently an integer of 0 to 2; ring B is an optionally substituted ring, provided that the two atoms constituting ring B, which are adjacent to the spiro carbon atom, are not oxygen atoms at the same time, or a salt thereof, or a prodrug thereof.
    本发明旨在提供一种新型SCD抑制剂。本发明涉及一种包括下式(I)所表示的化合物的SCD抑制剂:其中R是一个可选择取代的环基或可选择取代的氨甲酰基,但R不是一个可选择取代的7-吡啶并[2,3-d]嘧啶基团;环A是一个可选择进一步取代的吡啶并嘧啶环;R1、R2、R3、R4、R11、R12、R13和R14分别独立地是氢原子或取代基,或R1和R11的组合体,R2和R12的组合体,R3和R13的组合体,或R4和R14的组合体可选择形成氧基,或R2和R4的组合体可选择形成键或烷基交联;m和n分别独立地是0到2的整数;环B是一个可选择取代的环,但构成环B的两个与螺碳原子相邻的原子不同时为氧原子,或其盐,或其前药。
  • ORGANIC COMPOUNDS
    申请人:Dales Natalie
    公开号:US20110105530A1
    公开(公告)日:2011-05-05
    The present invention provides heterocyclic derivatives that modulate the activity of stearoyl-CoA desaturase. Methods of using such derivatives to modulate the activity of stearoyl-CoA desaturase and pharmaceutical compositions comprising such derivatives are also encompassed.
    本发明提供了可以调节硬脂酰-辅酶A脱饱和酶活性的杂环衍生物。本发明还涵盖了使用这些衍生物来调节硬脂酰-辅酶A脱饱和酶活性的方法和包含这些衍生物的药物组合物。
  • Organic compounds
    申请人:Dales Natalie
    公开号:US09187426B2
    公开(公告)日:2015-11-17
    The present invention provides heterocyclic derivatives that modulate the activity of stearoyl-CoA desaturase. Methods of using such derivatives to modulate the activity of stearoyl-CoA desaturase and pharmaceutical compositions comprising such derivatives are also encompassed.
    本发明提供了可以调节硬脂酰辅酶A去饱和酶活性的杂环衍生物。本发明还涵盖了使用这些衍生物来调节硬脂酰辅酶A去饱和酶活性的方法以及包含这些衍生物的制药组合物。
  • INHIBITORS OF UNDECAPRENYL PYROPHOSPHATE SYNTHASE
    申请人:Hurley Timothy Brian
    公开号:US20090203694A1
    公开(公告)日:2009-08-13
    The present invention relates to compounds that are selective and/or potent inhibitors of UPPS. In addition to compounds which inhibit UPPS, the invention also provides pharmaceutical compositions comprising these compounds and methods of using these compounds for treating bacterial disease, such as bacterial infection.
    本发明涉及一种选择性和/或强效抑制UPPS的化合物。除了抑制UPPS的化合物外,本发明还提供包含这些化合物的药物组合物以及使用这些化合物治疗细菌性疾病(如细菌感染)的方法。
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