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2-苯基-1,3-噻唑-4-羰酰氯 | 36094-04-9

中文名称
2-苯基-1,3-噻唑-4-羰酰氯
中文别名
2-苯基-1,3-噻唑-4-甲酰氯
英文名称
2-phenyl-1,3-thiazole-4-carboxylic acid chloride
英文别名
2-phenyl-1,3-thiazol-4-carbonyl chloride;2-phenyl-thiazole-4-carbonyl chloride;2-Phenyl-thiazol-4-carbonylchlorid;2-phenyl-thiazole-4-carboxylic acid chloride;2-phenyl-4-thiazolecarboxylic acid chloride;2-Phenyl-1,3-thiazole-4-carbonyl chloride
2-苯基-1,3-噻唑-4-羰酰氯化学式
CAS
36094-04-9
化学式
C10H6ClNOS
mdl
MFCD02681968
分子量
223.683
InChiKey
ZZFOIDMEHXGBKS-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:
    100 °C
  • 沸点:
    358.3±34.0 °C(Predicted)
  • 密度:
    1.365±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.5
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    58.2
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 危险品标志:
    C
  • 安全说明:
    S26,S36/37/39
  • 危险类别码:
    R34
  • 海关编码:
    2934100090
  • 危险品运输编号:
    UN 3261

SDS

SDS:66380e5a4c31aee667c8f60751739ba2
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Name: 2-Phenyl-1 3-thiazole-4-carbonyl chloride 97% Material Safety Data Sheet
Synonym:
CAS: 36094-04-9
Section 1 - Chemical Product MSDS Name:2-Phenyl-1 3-thiazole-4-carbonyl chloride 97% Material Safety Data Sheet
Synonym:

Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS
CAS# Chemical Name content EINECS#
36094-04-9 2-phenyl-1,3-thiazole-4-carbonyl chlor 97% unlisted
Hazard Symbols: C
Risk Phrases: 34

Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
Causes burns.Moisture sensitive.
Potential Health Effects
Eye:
Causes eye burns.
Skin:
Causes skin burns.
Ingestion:
Causes gastrointestinal tract burns.
Inhalation:
Causes chemical burns to the respiratory tract.
Chronic:
Not available.

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 immediately. Immediately flush skin with plenty of water for at least 15 minutes while removing contaminated clothing and shoes.
Ingestion:
Do not induce vomiting. Get medical aid immediately. Wash mouth out with water.
Inhalation:
Get medical aid immediately. Remove from exposure and move to fresh air immediately. If not breathing, give artificial respiration. If breathing is difficult, give oxygen.
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.
Extinguishing Media:
Use foam, dry chemical, or carbon dioxide.

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.

Section 7 - HANDLING and STORAGE
Handling:
Do not breathe dust, vapor, mist, or gas. Do not get in eyes, on skin, or on clothing. Use only in a chemical fume hood.
Storage:
Store in a cool, dry place. Store in a tightly closed container.
Corrosives area. Store under an inert atmosphere. Store under nitrogen.

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# 36094-04-9: Personal Protective Equipment Eyes: Not available.
Skin:
Wear appropriate protective gloves to prevent skin exposure.
Clothing:
Wear appropriate protective clothing to prevent skin exposure.
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: Solid
Color: brown
Odor: Not available.
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: Not available.
Freezing/Melting Point: 99 - 102 deg C
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: C10H6ClNOS
Molecular Weight: 223.68

Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Not available.
Conditions to Avoid:
Incompatible materials, exposure to moist air or water.
Incompatibilities with Other Materials:
Strong oxidizing agents, oxidizing agents, reducing agents, bases, alcohols, amines.
Hazardous Decomposition Products:
Hydrogen chloride, chlorine, nitrogen oxides, carbon monoxide, carbon dioxide, sulfur oxides (SOx), including sulfur oxide and sulfur dioxide.
Hazardous Polymerization: Has not been reported

Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 36094-04-9 unlisted.
LD50/LC50:
Not available.
Carcinogenicity:
2-phenyl-1,3-thiazole-4-carbonyl chloride - 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
Shipping Name: CORROSIVE SOLID, ACIDIC, ORGANIC, N.O.S.*
Hazard Class: 8
UN Number: 3261
Packing Group: III
IMO
Shipping Name: CORROSIVE SOLID, ACIDIC, ORGANIC, N.O.S.
Hazard Class: 8
UN Number: 3261
Packing Group: III
RID/ADR
Shipping Name: CORROSIVE SOLID, ACIDIC, ORGANIC, N.O.S.
Hazard Class: 8
UN Number: 3261
Packing group: III

Section 15 - REGULATORY INFORMATION

European/International Regulations
European Labeling in Accordance with EC Directives
Hazard Symbols: C
Risk Phrases:
R 34 Causes burns.
Safety Phrases:
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# 36094-04-9: No information available.
Canada
None of the chemicals in this product are listed on the DSL/NDSL list.
CAS# 36094-04-9 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 36094-04-9 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:
    2-苯基-1,3-噻唑-4-羰酰氯甲醇 、 sodium tetrahydroborate 、 三乙胺 作用下, 以 四氢呋喃二氯甲烷二丁醚 为溶剂, 反应 6.78h, 生成 1-(2-phenylthiazol-4-yl)ethanol
    参考文献:
    名称:
    [EN] IMIDAZOTHIADIAZOLE AND IMIDAZOPYRAZINE DERIVATIVES AS PROTEASE ACTIVATED RECEPTOR 4 (PAR4) INHIBITORS FOR TREATING PLATELET AGGREGATION
    [FR] DÉRIVÉS D'IMIDAZOTHIADIAZOLE ET D'IMIDAZOPYRAZINE UTILISÉS COMME INHIBITEURS DU RÉCEPTEUR 4 ACTIVÉ PAR UNE PROTÉASE (PAR4) POUR LE TRAITEMENT DE L'AGRÉGATION PLAQUETTAIRE
    摘要:
    本发明提供了式I的噻唑化合物,其中W、Y、R0、R2、R4、R5、R6、R7、X1、X2、X3和X4如本文所定义,或其立体异构体、互变异构体、药学上可接受的盐、前药酯或溶剂化合物形式,其中所有变量均如本文所定义。这些化合物是血小板聚集抑制剂,因此可用作治疗或预防血栓栓塞性疾病的药物。
    公开号:
    WO2013163279A1
  • 作为产物:
    描述:
    硫代苯甲酰胺草酰氯 、 sodium hydroxide 作用下, 以 甲醇乙醇二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 7.03h, 生成 2-苯基-1,3-噻唑-4-羰酰氯
    参考文献:
    名称:
    [EN] IMIDAZOTHIADIAZOLE AND IMIDAZOPYRAZINE DERIVATIVES AS PROTEASE ACTIVATED RECEPTOR 4 (PAR4) INHIBITORS FOR TREATING PLATELET AGGREGATION
    [FR] DÉRIVÉS D'IMIDAZOTHIADIAZOLE ET D'IMIDAZOPYRAZINE UTILISÉS COMME INHIBITEURS DU RÉCEPTEUR 4 ACTIVÉ PAR UNE PROTÉASE (PAR4) POUR LE TRAITEMENT DE L'AGRÉGATION PLAQUETTAIRE
    摘要:
    本发明提供了式I的噻唑化合物,其中W、Y、R0、R2、R4、R5、R6、R7、X1、X2、X3和X4如本文所定义,或其立体异构体、互变异构体、药学上可接受的盐、前药酯或溶剂化合物形式,其中所有变量均如本文所定义。这些化合物是血小板聚集抑制剂,因此可用作治疗或预防血栓栓塞性疾病的药物。
    公开号:
    WO2013163279A1
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文献信息

  • [EN] INDOLE AMIDE DERIVATIVES AND RELATED COMPOUNDS FOR USE IN THE TREATMENT OF NEURODEGENERATIVE DISEASES<br/>[FR] DÉRIVÉS D'INDOLAMIDE ET COMPOSÉS ASSOCIÉS DESTINÉS À ÊTRE UTILISÉS DANS LE TRAITEMENT DES MALADIES NEURODÉGÉNÉRATIVES
    申请人:UNIV LEUVEN KATH
    公开号:WO2010142801A1
    公开(公告)日:2010-12-16
    This invention provides novel compounds and the novel compounds for use as a medicine, more in particular for the prevention or treatment of neurodegenerative disorders, more specifically certain neurological disorders, such as disorders collectively known as tauopathies, and disorders characterised by cytotoxic α-synuclein amyloidogenesis. The present invention also relates to the use of said novel compounds for the manufacture of medicaments useful for treating such neurodegenerative disorders. The present invention further relates to pharmaceutical compositions including said novel compounds and to methods for the preparation of said novel compounds.
    本发明提供了新型化合物,以及这些新型化合物作为药物的使用,特别是用于预防或治疗神经退行性疾病,更具体地是一些神经系统疾病,例如统称为tauopathies的疾病,以及以细胞毒性α-突触核蛋白淀粉样蛋白生成为特征的疾病。本发明还涉及将所述新型化合物用于制造用于治疗此类神经退行性疾病的药物。本发明还涉及包括所述新型化合物的药物组合物,以及制备所述新型化合物的方法。
  • Decarbonylative Methylation of Aromatic Esters by a Nickel Catalyst
    作者:Toshimasa Okita、Kei Muto、Junichiro Yamaguchi
    DOI:10.1021/acs.orglett.8b01233
    日期:2018.5.18
    A Ni-catalyzed decarbonylative methylation of aromatic esters was achieved using methylaluminums as methylating agents. Dimethylaluminum chlorides uniquely worked as the methyl source. Because of the Lewis acidity of aluminum reagents, less reactive alkyl esters could also undergo the present methylation. By controlling the Lewis acidity of aluminum reagents, a chemoselective decarbonylative cross-coupling
    使用甲基铝作为甲基化剂,可以实现镍催化的芳香族酯的脱羰甲基化。氯化二甲基铝独特地用作甲基源。由于铝试剂的路易斯酸度,反应性较低的烷基酯也可能会发生本甲基化。通过控制铝试剂的路易斯酸度,烷基酯和苯基酯之间的化学选择性脱羰交联是成功的。
  • 4,4-difluoro-2,3,4,5-tetrahydro-1H-1-benzoazepine derivatives and drug compositions containing them
    申请人:Yamanouchi Pharmaceutical Co., Ltd.
    公开号:US06340678B1
    公开(公告)日:2002-01-22
    4,4-difluoro-2,3,4,5-tetrahydro-1H-1-benzoazepine compounds or salts thereof and pharmaceutical compositions containing 4,4-difluoro-2,3,4,5-tetrahydro-1H-1-benzoazepine compounds, or salts thereof, and a pharmaceutically acceptable carrier. The chemical structure of these compounds is characterized by a difluoro group on a ring carbon atom adjacent to an azepine ring carbon atom substituted with a methylidene group. Pharmaceutical compositions containing these compounds are particularly useful as oxytocin antagonists and are effective in inhibiting threatened premature birth or abortion and precesarean birth, and are effective as a remedy for dysmenorrhea and other such conditions.
    4,4-二氟-2,3,4,5-四氢-1H-1-苯并氮杂环化合物或其盐,以及含有4,4-二氟-2,3,4,5-四氢-1H-1-苯并氮杂环化合物或其盐和药用辅料的药物组合物。这些化合物的化学结构特点是在与氮杂环碳原子相邻的环碳原子上有一个二氟基团,该氮杂环碳原子被甲基亚基团取代。含有这些化合物的药物组合物特别用作催产素拮抗剂,在抑制早产或流产、以及前置胎盘分娩方面有效,并且作为治疗痛经和其他此类病症的药物有效。
  • Amide compounds
    申请人:Fujisawa Pharmaceutical Co., Ltd.
    公开号:US06770667B1
    公开(公告)日:2004-08-03
    The present invention is a compound and pharmaceutical composition comprising a compound of formula (I): wherein R1 is a 4-(lower) alkyl-imidazol-1-yl or a 4,5-di(lower) alkyl-imidazol-1-yl group, R2 is a hydrogen atom or a lower alkyl group, and R3 is a fluorenyl group. The compound of formula (I) includes pharmaceutically acceptable salts: The compound of formula (I) and salts thereof have 5-HT antagonism activity.
    本发明是一种化合物和药物组合物,包括式(I)的化合物:其中R1是4-(较低)烷基-咪唑-1-基或4,5-二(较低)烷基-咪唑-1-基基团,R2是氢原子或较低烷基基团,R3是芴基团。式(I)的化合物包括药用可接受的盐:式(I)的化合物及其盐具有5-HT拮抗活性。
  • PHENYLPROPIONIC ACID DERIVATIVE AND USE THEREOF
    申请人:MORITA Kohei
    公开号:US20100093819A1
    公开(公告)日:2010-04-15
    A compound represented by the following general formula (1) or a salt thereof, which has superior inhibitory activity against type 4 PLA 2 , and thus has prostaglandin and/or leucotriene production suppressing action [X represents a halogen atom, an alkyl group which may be substituted, or the like, Y represents hydrogen atom or an alkyl group which may be substituted, and Z represents hydrogen atom or an alkyl group which may be substituted].
    由以下一般式(1)表示的化合物或其盐,具有优越的抑制对4型PLA2的活性,因此具有前列腺素和/或白三烯产生抑制作用【X代表卤素原子、可能被取代的烷基或类似物,Y代表氢原子或可能被取代的烷基,Z代表氢原子或可能被取代的烷基】。
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