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37131-87-6

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37131-87-6 Usage

Description

5-BROMOPYRIMIDINE-2-CARBOXYLIC ACID is an organic compound that serves as a crucial intermediate in various chemical syntheses. It is characterized by its unique molecular structure, which features a pyrimidine ring with a carboxyl group and a bromine atom at the 5th position. 5-BROMOPYRIMIDINE-2-CARBOXYLIC ACID is known for its versatility in chemical reactions and its ability to be incorporated into a wide range of products.

Uses

Used in the Agrochemical Industry:
5-BROMOPYRIMIDINE-2-CARBOXYLIC ACID is used as an important raw material and intermediate for the synthesis of various agrochemicals. Its unique chemical properties allow it to be incorporated into the development of new pesticides, herbicides, and other agricultural chemicals that can help improve crop yields and protect plants from pests and diseases.
Used in the Pharmaceutical Industry:
In the pharmaceutical sector, 5-BROMOPYRIMIDINE-2-CARBOXYLIC ACID is utilized as a key intermediate in the synthesis of various drugs. Its molecular structure can be modified and combined with other compounds to create new pharmaceuticals with potential therapeutic applications, such as antibiotics, antivirals, and other therapeutic agents.
Used in the Dyestuff Industry:
5-BROMOPYRIMIDINE-2-CARBOXYLIC ACID is also employed in the dyestuff industry as a vital intermediate for the production of various dyes and pigments. Its unique chemical properties enable the creation of a wide range of colors and shades, which can be used in various applications, such as textiles, plastics, and printing inks.

Check Digit Verification of cas no

The CAS Registry Mumber 37131-87-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,1,3 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 37131-87:
(7*3)+(6*7)+(5*1)+(4*3)+(3*1)+(2*8)+(1*7)=106
106 % 10 = 6
So 37131-87-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H3BrN2O2/c6-3-1-7-4(5(9)10)8-2-3/h1-2H,(H,9,10)

37131-87-6 Well-known Company Product Price

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  • Alfa Aesar

  • (H64041)  5-Bromopyrimidine-2-carboxylic acid, 98%   

  • 37131-87-6

  • 250mg

  • 228.0CNY

  • Detail
  • Alfa Aesar

  • (H64041)  5-Bromopyrimidine-2-carboxylic acid, 98%   

  • 37131-87-6

  • 1g

  • 682.0CNY

  • Detail
  • Alfa Aesar

  • (H64041)  5-Bromopyrimidine-2-carboxylic acid, 98%   

  • 37131-87-6

  • 5g

  • 2479.0CNY

  • Detail

37131-87-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Bromopyrimidine-2-carboxylic Acid

1.2 Other means of identification

Product number -
Other names 5-bromopyrimidine-2-carboxylic acid

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:37131-87-6 SDS

37131-87-6Relevant articles and documents

Spirocyclic delta opioid receptor agonists for the treatment of pain: Discovery of N,N-diethyl-3-hydroxy-4-(spiro[chromene-2,4′-piperidine]-4- yl) benzamide (ADL5747)

Bourdonnec, Bertrand Le,Windh, Rolf T.,Leister, Lara K.,Zhou, Q. Jean,Ajello, Christopher W.,Gu, Minghua,Chu, Guo-Hua,Tuthill, Paul A.,Barker, William M.,Koblish, Michael,Wiant, Daniel D.,Graczyk, Thomas M.,Belanger, Serge,Cassel, Joel A.,Feschenko, Marina S.,Brogdon, Bernice L.,Smith, Steven A.,Derelanko, Michael J.,Kutz, Steve,Little, Patrick J.,Dehaven, Robert N.,DeHaven-Hudkins, Diane L.,Dolle, Roland E.

experimental part, p. 5685 - 5702 (2010/02/28)

Selective, nonpeptidic δ opioid receptor agonists have been the subject of great interest as potential novel analgesic agents. The discoveries of BW373U86 (1) and SNC80 (2) contributed to the rapid expansion of research in this field. However, poor drug-like properties and low therapeutic indices have prevented clinical evaluation of these agents. Doses of 1 and 2 similar to those required for analgesic activity produce convulsions in rodents and nonhuman primates. Recently, we described a novel series of potent, selective, and orally bioavailable delta opioid receptor agonists. The lead derivative, ADL5859 (4), is currently in phase II proof-of-concept studies for the management of pain. Further structure activity relationship exploration has led to the discovery of ADL5747 (36), which is approximately 50-fold more potent than 4 in an animal model of inflammatory pain. On the basis of its favorable efficacy, safety, and pharmacokinetic profile, 36 was selected as a clinical candidate for the treatment of pain.

SUBSTITUTED TRIAZOLE DERIVATIVES AS OXYTOCIN ANTAGONISTS

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Page/Page column 87-88, (2010/02/11)

The present invention relates to a class of substituted 1,2,4-triazoles of formula (I) with activity as oxytocin antagonists, uses thereof, processes for the preparation thereof and compositions containing, said, inhibitors. These inhibitors have utility in a variety of therapeutic areas including sexual dysfunction, particularly premature ejaculation (P.E.).

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