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50477-28-6

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50477-28-6 Usage

General Description

5,7-Dibromo-1H-indazole is a chemical compound classified under the family of Indazoles. It is known for its two Bromine substituents at the 5th and 7th positions of the indazole base structure. 5,7-Dibromo-1H-indazole, with a molecular formula of C7H4Br2N2, finds its uses in various research or experimental applications such as organic synthesis and pharmaceutical research. Properties of this compound, including its stability, potential reactions, and health hazards, can be explored depending on its specific applications, though safety precautions must always be considered when handling. It is commonly stored in a cool, dry place in a tightly closed container.

Check Digit Verification of cas no

The CAS Registry Mumber 50477-28-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,4,7 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 50477-28:
(7*5)+(6*0)+(5*4)+(4*7)+(3*7)+(2*2)+(1*8)=116
116 % 10 = 6
So 50477-28-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H4Br2N2/c8-5-1-4-3-10-11-7(4)6(9)2-5/h1-3H,(H,10,11)

50477-28-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,7-Dibromo-1H-indazole

1.2 Other means of identification

Product number -
Other names 5,7-DIBROMO-1H-INDAZOLE

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:50477-28-6 SDS

50477-28-6Downstream Products

50477-28-6Relevant articles and documents

Efficient and scalable synthesis of 3,5,7-trisubstituted 1H-indazoles as potent IKK2 inhibitors

Lin, Xichen,Busch-Petersen, Jakob,Deng, Jianghe,Edwards, Christine,Zhang, Zhaoguo,Kerns, Jeffrey K.

scheme or table, p. 3216 - 3220 (2009/06/18)

Efficient and scalable chemical approaches to 3,5,7-trisubstituted 1H-indazoles were developed and applied to the synthesis of 1,1-dimethylethyl 4-[7-(aminocarbonyl)-5-bromo-1H-indazol-3-yl]-1-piperidinecarboxylate, a key intermediate for 3,5,7-trisubstit

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