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3-氰基-2-巯基-6-甲基吡啶-4-甲酸乙酯 | 56891-69-1

中文名称
3-氰基-2-巯基-6-甲基吡啶-4-甲酸乙酯
中文别名
3-氰基-2-巯基-6-甲基吡啶-4-羧酸乙酯
英文名称
3-cyano-2-mercapto-6-methylisonicotinic acid ethyl ester
英文别名
ethyl 3-cyano-2-mercapto-6-methylpyridine-4-carboxylate;ethyl 3-cyano-6-methyl-2-sulfanylpyridine-4-carboxylate
3-氰基-2-巯基-6-甲基吡啶-4-甲酸乙酯化学式
CAS
56891-69-1
化学式
C10H10N2O2S
mdl
MFCD00052275
分子量
222.268
InChiKey
WBMMFDGNOQLZNF-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:
    214 °C
  • 沸点:
    302.8±52.0 °C(Predicted)
  • 密度:
    1.29±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1
  • 重原子数:
    15
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    94.2
  • 氢给体数:
    1
  • 氢受体数:
    4

安全信息

  • 危险等级:
    6.1
  • 危险品标志:
    Xn
  • 安全说明:
    S26,S36/37/39
  • 危险类别码:
    R20/21/22,R36/37/38
  • 海关编码:
    2933399090
  • 包装等级:
    III
  • 危险类别:
    6.1
  • 危险品运输编号:
    UN 3276
  • 储存条件:
    存于室温下,密封保存,并确保环境干燥。

SDS

SDS:a885053c7cc9ef225b89c0c7de84ac03
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Name: Ethyl 3-cyano-2-mercapto-6-Ethyl 3-cyano-2-mercapto-6- 97% Material Safety Data Sheet
Synonym: Ethyl 3-cyano-2-mercapto-6-methylpyridine-4-carboxylat
CAS: 56891-69-1
Section 1 - Chemical Product MSDS Name:Ethyl 3-cyano-2-mercapto-6-Ethyl 3-cyano-2-mercapto-6- 97% Material Safety Data Sheet
Synonym:Ethyl 3-cyano-2-mercapto-6-methylpyridine-4-carboxylat

Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS
CAS# Chemical Name content EINECS#
56891-69-1 Ethyl 3-cyano-2-mercapto-6-methylisoni 97% unlisted
Hazard Symbols: XN
Risk Phrases: 20/21/22 36/37/38

Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
Harmful by inhalation, in contact with skin and if swallowed.
Irritating to eyes, respiratory system and skin.
Potential Health Effects
Eye:
Causes eye irritation.
Skin:
Causes skin irritation. Harmful if absorbed through the skin.
Ingestion:
Harmful if swallowed. May cause irritation of the digestive tract.
Inhalation:
Harmful if inhaled. Causes respiratory tract irritation.
Chronic:
Not available.

Section 4 - FIRST AID MEASURES
Eyes: Flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids. Get medical aid.
Skin:
Get medical aid. Flush skin with plenty of water for at least 15 minutes while removing contaminated clothing and shoes.
Ingestion:
Get medical aid. Wash mouth out with water.
Inhalation:
Remove from exposure and move to fresh air immediately. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Get medical aid.
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 water spray, dry chemical, carbon dioxide, or chemical 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.

Section 7 - HANDLING and STORAGE
Handling:
Avoid breathing dust, vapor, mist, or gas. Avoid contact with skin and eyes.
Storage:
Store in a cool, dry place. Store in a tightly closed container.

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# 56891-69-1: 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: orange
Odor: Not available.
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: Not available.
Freezing/Melting Point: 214 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: C10H10N2O2S
Molecular Weight: 222

Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Not available.
Conditions to Avoid:
Incompatible materials.
Incompatibilities with Other Materials:
Oxidizing agents, bases, acid chlorides, amines.
Hazardous Decomposition Products:
Nitrogen oxides, carbon monoxide, oxides of sulfur, carbon dioxide.
Hazardous Polymerization: Has not been reported

Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 56891-69-1 unlisted.
LD50/LC50:
Not available.
Carcinogenicity:
Ethyl 3-cyano-2-mercapto-6-methylisonicotinate - 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: NITRILES, SOLID, TOXIC, N.O.S.*
Hazard Class: 6.1
UN Number: 3276
Packing Group: III
IMO
Shipping Name: NITRILES, TOXIC, N.O.S.
Hazard Class: 6.1
UN Number: 3276
Packing Group: III
RID/ADR
Shipping Name: NITRILES, TOXIC, N.O.S.
Hazard Class: 6.1
UN Number: 3276
Packing group: III

Section 15 - REGULATORY INFORMATION

European/International Regulations
European Labeling in Accordance with EC Directives
Hazard Symbols: XN
Risk Phrases:
R 20/21/22 Harmful by inhalation, in contact with
skin and if swallowed.
R 36/37/38 Irritating to eyes, respiratory system
and skin.
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.
WGK (Water Danger/Protection)
CAS# 56891-69-1: No information available.
Canada
None of the chemicals in this product are listed on the DSL/NDSL list.
CAS# 56891-69-1 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 56891-69-1 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:
    参考文献:
    名称:
    [EN] SUBSTITUTED 3-AMINO-THIENO[2,3-b]PYRIDINE-2-CARBOXYLIC ACID AMIDE COMPOUNDS AND PROCESSES FOR PREPARING AND THEIR USES
    [FR] COMPOSES AMIDE D'ACIDE 3-AMINO-THIENO[2,3-b]PYRIDINE-2-CARBOXYLIQUE SUBSTITUES ET PROCESSUS DE PREPARATION ET D'UTILISATION DE CES COMPOSES
    摘要:
    公开的是式(I)的化合物,其中R1和R2如本文所定义,这些化合物可用作IκB激酶(IKK)复合物激酶活性的抑制剂。因此,这些化合物在治疗IKK介导的疾病,包括自身免疫疾病、炎症性疾病和癌症方面是有用的。还公开了包含这些化合物的药物组合物以及制备这些化合物的方法。
    公开号:
    WO2003103661A1
  • 作为产物:
    描述:
    2-氯-3-氰基-6-甲基异烟酸乙酯硫脲 作用下, 以 乙醇 为溶剂, 反应 24.0h, 以50%的产率得到3-氰基-2-巯基-6-甲基吡啶-4-甲酸乙酯
    参考文献:
    名称:
    [EN] SUBSTITUTED 3-AMINO-THIENO[2,3-b]PYRIDINE-2-CARBOXYLIC ACID AMIDE COMPOUNDS AND PROCESSES FOR PREPARING AND THEIR USES
    [FR] COMPOSES AMIDE D'ACIDE 3-AMINO-THIENO[2,3-b]PYRIDINE-2-CARBOXYLIQUE SUBSTITUES ET PROCESSUS DE PREPARATION ET D'UTILISATION DE CES COMPOSES
    摘要:
    公开的是式(I)的化合物,其中R1和R2如本文所定义,这些化合物可用作IκB激酶(IKK)复合物激酶活性的抑制剂。因此,这些化合物在治疗IKK介导的疾病,包括自身免疫疾病、炎症性疾病和癌症方面是有用的。还公开了包含这些化合物的药物组合物以及制备这些化合物的方法。
    公开号:
    WO2003103661A1
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文献信息

  • AZOLOPYRIDIN-3-ONE DERIVATIVES AS INHIBITORS OF LIPASES AND PHOSPHOLIPASES
    申请人:Petry Stefan
    公开号:US20130157941A1
    公开(公告)日:2013-06-20
    The present invention relates to azolopyridin-3-one derivatives of the general formula (I) with the meanings specified in the description, to their pharmaceutically usable salts and to their use as drug substances.
    本发明涉及通式(I)所示的咪唑吡啶-3-酮衍生物,其含义如描述中所指定的,以及它们的药用盐和作为药物物质的用途。
  • Methods for treating Hepatitis C
    申请人:Karp Mitchell Gary
    公开号:US20060019976A1
    公开(公告)日:2006-01-26
    In accordance with the present invention, compounds that can inhibit viral replication, preferably Hepatitis C Virus (HCV) replication, have been identified, and methods for their use provided. In one aspect of the invention, compounds useful in the treatment or prevention of a viral infection are provided. In another aspect of the invention, compounds useful in the treatment or prevention of HCV infection are provided.
    根据本发明,已经确定了一些可以抑制病毒复制的化合物,优选是乙型肝炎病毒(HCV)复制,并提供了它们的使用方法。在本发明的一个方面,提供了用于治疗或预防病毒感染的化合物。在本发明的另一个方面,提供了用于治疗或预防HCV感染的化合物。
  • Substituted ethyl 2-acyl-3-amino-6-methylthieno[2,3-<i>b</i>]pyridine-4-carboxylates as synthons for novel heterocycles
    作者:Frank T. Coppo、Maged M. Fawzi
    DOI:10.1002/jhet.5570340304
    日期:1997.5
    The triethylamine-catalyzed reaction of 4-substituted ethyl 2-acyl-3-amino-6-methylthieno[2,3-b]pyridine-4-carboxylates IIIa-h with 2,2,6-trimethyl-4H-1,3-dioxin-4-one IV gave 4-substituted ethyl 3-acetyl-2-hydroxy-7-methylthieno[2,3-b:4,5-b′]dipyridine-9-carboxylates Va-h. Some of the thienodipyridines (V) reacted with excess IV to give 5-substituted ethyl 3-acetyl-4,8-dimethyl-2-oxo-2H-pyrano[2,3-b]-pyrido[3′
    三乙胺催化的4-取代的2-酰基-3-氨基-6-甲基硫代[2,3 - b ]吡啶-4-羧酸乙酯IIIa-h与2,2,6-三甲基-4 H -1的反应, 3-二恶英-4-酮IV给出4-取代的乙基3-乙酰基-2-羟基-7-甲基噻吩并[2,3- b:4,5 - b ']二吡啶-9-羧酸盐Va-h。一些噻二吡啶(V)与过量的IV反应生成5-取代的乙基3-乙酰基-4,8-​​二甲基-2-氧代-2H-吡喃并[2,3- b ]-吡啶并[3',2': 4,5]噻吩并[2,3 - e ]吡啶-10-羧酸酯VI。
  • Substituted 3-amino-thieno[2,3-b]pyridine-2-carboxylic acid amide compounds and processes for preparing and their uses
    申请人:Cywin L. Charles
    公开号:US20050288285A1
    公开(公告)日:2005-12-29
    Disclosed are compounds of formula (I): wherein R 1 and R 2 are defined herein, which are useful as inhibitors of the kinase activity of the IκB kinase (IKK) complex. The compounds are therefore useful in the treatment of IKK mediated diseases including autoimmune diseases inflammatory diseases and cancer. Also disclosed are pharmaceutical compositions comprising these compounds and processes for preparing these compounds.
    本发明涉及化合物(I)的公开,其中R1和R2在此定义,这些化合物可用作IκB激酶(IKK)复合物的激酶活性抑制剂。因此,这些化合物可用于治疗由IKK介导的疾病,包括自身免疫性疾病、炎症性疾病和癌症。还公开了包含这些化合物的药物组合物和制备这些化合物的过程。
  • Oxazolidinone combinatorial libraries, compositions and methods of preparation
    申请人:Gordeev F. Mikhail
    公开号:US20050004174A1
    公开(公告)日:2005-01-06
    Oxazolidinones and methods for their synthesis are provided. Also provided are combinatorial libraries comprising oxazolidinones, and methods to prepare the libraries. Further provided are methods of making biologically active oxazolidinones as well as pharmaceutically acceptable compositions comprising the oxazolidinones. The methods of library preparation include the attachment of oxazolidinones to a solid support. The methods of compound preparation in one embodiment involve the reaction of an iminophosphorane with a carbonyl containing polymeric support.
    本发明提供了氧杂环丙烷酮及其合成方法。还提供了包含氧杂环丙烷酮的组合化学文库以及制备这些文库的方法。此外,还提供了制备生物活性氧杂环丙烷酮的方法以及包含氧杂环丙烷酮的药学可接受组合物的方法。文库制备的方法包括将氧杂环丙烷酮附着到固体支持上。在一种实施例中,化合物制备的方法涉及将亚胺磷酰胺与含有羰基的聚合物支持物反应。
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