107263-89-8

• 

• Basic information

  1. Product Name: Thiazole, 4-ethynyl-2-methyl-
  2. Synonyms: Thiazole, 4-ethynyl-2-methyl-;4-Ethynyl-2-Methylthiazole
  3. CAS NO:107263-89-8
  4. Molecular Formula: C₆H₅NS
  5. Molecular Weight: 123.18
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 107263-89-8.mol
  9. Article Data: 6

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
  8. Solubility: N/A
  9. CAS DataBase Reference: Thiazole, 4-ethynyl-2-methyl-(CAS DataBase Reference)
  10. NIST Chemistry Reference: Thiazole, 4-ethynyl-2-methyl-(107263-89-8)
  11. EPA Substance Registry System: Thiazole, 4-ethynyl-2-methyl-(107263-89-8)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 107263-89-8(Hazardous Substances Data)

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• 4-ETHYNYL-2-METHYLTHIAZOLE

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• Hangzhou J&H Chemical Co., Ltd.
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• CAS107263-89-8 Thiazole, 4-ethynyl-2-methyl-

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• 4-ETHYNYL-2-METHYLTHIAZOLE CAS NO.107263-89-8

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107263-89-8 Usage

General Description

4-Ethynyl-2-methyl-thiazole is a specialized organic synthetic compound classified under the family of thiazoles, which are aromatic compounds with a ring made from one sulfur atom, one nitrogen atom, and three carbon atoms. It is notably used in the creation of pharmaceuticals and agrochemicals. Thiazoles are often used in medicinal chemistry due to their biological and pharmaceutical properties that can help in treating diseases. Proper handling and usage of 4-Ethynyl-2-methyl-thiazole are recommended due to its potential reactivity, as with any synthetic chemical compounds, but more precise toxicological properties specifically for this chemical could not be determined as they are not publicly listed or easily accessible.

Check Digit Verification of cas no

The CAS Registry Mumber 107263-89-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,2,6 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 107263-89:
(8*1)+(7*0)+(6*7)+(5*2)+(4*6)+(3*3)+(2*8)+(1*9)=118
118 % 10 = 8
So 107263-89-8 is a valid CAS Registry Number.

107263-89-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	4-Ethynyl-2-methylthiazole

1.2 Other means of identification

Product number	-
Other names	4-Ethynyl-2-methyl-1,3-thiazole

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:107263-89-8 SDS

107263-89-8Upstream product

• 107263-81-0 4-acetyl-2-methylthiazole semicarbazone 
• 23002-78-0 4-acetyl-2-methylthiazole 
• 6436-59-5 ethyl 2-methylthiazole-4-carboxylate 
• 329203-85-2 2-methyl-4-[(trimethylsilyl)ethynyl]-1,3-thiazole 
• 90965-06-3 dimethyl 1-(1-diazo-2-oxopropyl)phosphonate 
• 20949-84-2 2-methylthiazole-4-carbaldehyde 
• 107263-88-7 4-(2-Methyl-4-thiazolyl)1,2,3-selenadiazoles 

107263-89-8Downstream Products

107263-89-8Relevant articles and documents

HETEROCYCLIC COMPOUNDS AND USES THEREOF

-

Paragraph 00655; 00659; 00709, (2015/04/22)

Compounds and pharmaceutical compositions that modulate kinase activity, including PI3 kinase activity, and compounds, pharmaceutical compositions, and methods of treatment of diseases and conditions associated with kinase activity, including PI3 kinase activity, are described herein.

NOVEL HETEROCYCLIC DERIVATIVES AS M-GLU5 ANTAGONISTS

-

Page/Page column 38, (2009/03/07)

This invention relates to novel heterocyclic compounds having selective affinity for the mGlu5 subtype of metabotropic receptors, pharmaceutical compositions thereof and uses for such compounds and compositions in the treatment of lower urinary tract diso

Design, synthesis and biological evaluation of novel, simplified analogues of laulimalide: Modification of the side chain

Paterson, Ian,Menche, Dirk,Hakansson, Anders E.,Longstaff, Adrian,Wong, David,Barasoain, Isabel,Buey, Ruben M.,Diaz, J. Fernando

, p. 2243 - 2247 (2007/10/03)

Novel, simplified analogues of the microtubule-stabilizing anticancer agent laulimalide, including the first derivatives with unnatural side chains, were designed by molecular modelling, synthesized by a late-stage diversification strategy, and evaluated in vitro for growth inhibition of human ovarian carcinoma cell lines (A2780, A2780/AD10).

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