183988-30-9

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• Basic information

  1. Product Name: N-(4-BROMO-1-METHYL-1H-PYRAZOL-5-YL)-2-CHLOROACETAMIDE, TECH
  2. Synonyms: N-(4-BROMO-1-METHYL-1H-PYRAZOL-5-YL)-2-CHLOROACETAMIDE, TECH
  3. CAS NO:183988-30-9
  4. Molecular Formula: C₆H₇BrClN₃O
  5. Molecular Weight: 252.49628
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 183988-30-9.mol
  9. Article Data: 1

• 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.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: N-(4-BROMO-1-METHYL-1H-PYRAZOL-5-YL)-2-CHLOROACETAMIDE, TECH(CAS DataBase Reference)
  10. NIST Chemistry Reference: N-(4-BROMO-1-METHYL-1H-PYRAZOL-5-YL)-2-CHLOROACETAMIDE, TECH(183988-30-9)
  11. EPA Substance Registry System: N-(4-BROMO-1-METHYL-1H-PYRAZOL-5-YL)-2-CHLOROACETAMIDE, TECH(183988-30-9)

• 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: 183988-30-9(Hazardous Substances Data)

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• N-(4-Bromo-1-methyl-1H-pyrazol-5-yl)-2-chloroacetamide

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• N-(4-BROMO-1-METHYL-1H-PYRAZOL-5-YL)-2-CHLOROACETAMIDE

  Cas No: 183988-30-9

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183988-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183988-30-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,9,8 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 183988-30:
(8*1)+(7*8)+(6*3)+(5*9)+(4*8)+(3*8)+(2*3)+(1*0)=189
189 % 10 = 9
So 183988-30-9 is a valid CAS Registry Number.

183988-30-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name	N-(4-bromo-2-methylpyrazol-3-yl)-2-chloroacetamide

1.2 Other means of identification

Product number	-
Other names	Acetamide,N-(4-bromo-1-methyl-1H-pyrazol-5-yl)-2-chloro

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:183988-30-9 SDS

183988-30-9Upstream product

• 79-04-9 chloroacetyl chloride 
• 105675-85-2 4-bromo-2-methyl-2H-pyrazol-3-ylamine 

183988-30-9Downstream Products

• 183988-44-5 N-(4-Bromo-2-methyl-2H-pyrazol-3-yl)-2-(2-oxo-2-phenyl-ethylsulfanyl)-acetamide 

183988-30-9Relevant articles and documents

ACAT inhibitors derived from hetero-Diels-Alder cycloadducts of thioaldehydes

Wilde, Richard G.,Billheimer, Jeffrey T.,Germain, Sandie J.,Hausner, Elizabeth A.,Meunier, Paul C.,Munzer, Deborah A.,Stoltenborg, Janet K.,Gillies, Peter J.,Burcham, Deborah L.,Huang, Shiew-Mai,Klaczkiewicz, John D.,Ko, Soo S.,Wexler, Ruth R.

, p. 1493 - 1513 (2007/10/03)

Acyl-CoA:cholesterol acyltransferase (ACAT) is the enzyme largely responsible for intracellular cholesteror esterification. A systemic inhibitor of ACAT is believed to be able to slow or even reverse the atherosclerotic process. Towards that goal, a series of cyclic sulfides, derived from the hetero-Diels-Alder reaction of thioaldehydes with 1,3-dienes, and bearing carboxamide substituents, were prepared and evaluated for in vitro (in several tissues and species) and ex vivo ACAT inhibition. Minor changes in subsequent structure were found to have a significant effect in optimization of the biological activity of this series of compounds.

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