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1037298-05-7

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1037298-05-7 Usage

General Description

3-Bromo-4-iodophenol 97% is a chemical compound with a high purity level of 97%. It is a derivative of phenol that contains bromine and iodine atoms attached to the aromatic ring. 3-Bromo-4-iodophenol 97% is commonly used as a building block in organic synthesis and pharmaceutical research. It has potential applications in the development of new drugs, agrochemicals, and other fine chemicals. Additionally, its high purity level makes it suitable for use in analytical and research purposes, where accurate and consistent results are essential. Overall, 3-Bromo-4-iodophenol 97% is a versatile chemical with various potential applications in the field of chemistry and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 1037298-05-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,7,2,9 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1037298-05:
(9*1)+(8*0)+(7*3)+(6*7)+(5*2)+(4*9)+(3*8)+(2*0)+(1*5)=147
147 % 10 = 7
So 1037298-05-7 is a valid CAS Registry Number.

1037298-05-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromo-4-iodo-phenol

1.2 Other means of identification

Product number -
Other names 3-bromo-4-imino-3-cyano-1,2,3,4-tetrahydrospiro(naphthalene-2,1'-cyclohexane)

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:1037298-05-7 SDS

1037298-05-7Relevant articles and documents

Synthesis of substituted indoline and carbazole by benzyne-mediated cyclization-functionalization

Noji, Toshiharu,Fujiwara, Hideto,Okano, Kentaro,Tokuyama, Hidetoshi

supporting information, p. 1946 - 1949 (2013/06/04)

A benzyne-mediated synthesis of substituted indolines and carbazoles was developed. The reaction includes generation of benzyne using Mg(TMP) 2·2LiCl as a base, cyclization, and trapping the resulting organomagnesium intermediate with an electr

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