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1152475-42-7

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1152475-42-7 Usage

General Description

7-Bromo-2-chlorothieno[3,2-d]pyrimidine is a chemical compound with the molecular formula C6H3BrClN2S. It is a heterocyclic compound consisting of a thieno and pyrimidine ring with bromine and chlorine substituents. 7-Bromo-2-chlorothieno[3,2-d]pyrimidine is primarily used in pharmaceutical and agrochemical applications as a building block for the synthesis of various biologically active molecules. It is also used in research and development of new drugs and materials. The chemical properties and structure of 7-Bromo-2-chlorothieno[3,2-d]pyrimidine make it a versatile and valuable compound in the field of organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 1152475-42-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,2,4,7 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1152475-42:
(9*1)+(8*1)+(7*5)+(6*2)+(5*4)+(4*7)+(3*5)+(2*4)+(1*2)=137
137 % 10 = 7
So 1152475-42-7 is a valid CAS Registry Number.

1152475-42-7SDS

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 7-Bromo-2-chlorothieno[3,2-d]pyrimidine

1.2 Other means of identification

Product number -
Other names QC-737

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:1152475-42-7 SDS

1152475-42-7Relevant articles and documents

Identification of Thieno[3,2- d]pyrimidine Derivatives as Dual Inhibitors of Focal Adhesion Kinase and FMS-like Tyrosine Kinase 3

Cho, Hanna,Choi, Hwan Geun,Jeon, Eunhye,Kim, Nam Doo,Kim, Sunghoon,Kim, Younghoon,Kwon, Nam Hoon,Lee, Jiwon,Moon, Youngji,Ryu, Seongshick,Shin, Injae,Sim, Taebo,Song, Chiman,Yoon, Hojong

, p. 11934 - 11957 (2021/08/20)

Focal adhesion kinase (FAK) is overexpressed in highly invasive and metastatic cancers. To identify novel FAK inhibitors, we designed and synthesized various thieno[3,2-d]pyrimidine derivatives. An intensive structure-activity relationship (SAR) study led

FUSED RING PYRIMIDINE COMPOUND, INTERMEDIATE, AND PREPARATION METHOD, COMPOSITION AND USE THEREOF

-

Paragraph 0368-0369, (2018/08/12)

Disclosed area fused ring pyrimidine compound, and an intermediate, a preparation method, a composition and a use thereof. The fused ring pyrimidine compound is a compound as shown in formula I, a tautomer, an enantiomer, a diastereoisomer, a pharmaceutically acceptable salt, a metabolite, a metabolic precursor or a prodrug thereof, wherein the above-mentioned compound is used for the preparation of a medicine for preventing, remitting or treating one or more of immune system diseases, autoimmune diseases, cell proliferative diseases, allergic disorders and cardiovascular diseases, and the compound has a strong inhibitory effect on the Janues kinase, FGFR kinase, FLT3 kinase and Src family kinase.

COMPOUNDS THAT MODULATE EGFR ACTIVITY AND METHODS FOR TREATING OR PREVENTING CONDITIONS THEREWITH

-

, (2011/07/09)

Provided are compounds and methods for treating or preventing kinase-mediated disorders therewith.

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