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1032231-26-7

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1032231-26-7 Usage

Family

Benzene family

Atoms present

Bromine (Br), Iodine (I), and Sulfur (S) atoms

Functional group

Methylthio (-SCH3) group attached to the benzene ring

Usage

Organic synthesis, potential pharmaceutical and agrochemical applications

Physical state

Yellow crystalline solid at room temperature

Odor

Strong aromatic odor

Hazardous nature

Considered a hazardous chemical

Handling

Should be handled with care in a controlled laboratory setting

Check Digit Verification of cas no

The CAS Registry Mumber 1032231-26-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,2,2,3 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1032231-26:
(9*1)+(8*0)+(7*3)+(6*2)+(5*2)+(4*3)+(3*1)+(2*2)+(1*6)=77
77 % 10 = 7
So 1032231-26-7 is a valid CAS Registry Number.

1032231-26-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-4-iodo-2-(methylthio)benzene

1.2 Other means of identification

Product number -
Other names -

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:1032231-26-7 SDS

1032231-26-7Downstream Products

1032231-26-7Relevant articles and documents

t-BuOK-promoted methylthiolation of aryl fluorides with dimethyldisulfide under transition-metal-free and mild conditions

Huang, Dayun,Wu, Xiangmei

, (2021)

In the presence of potassium tert-butoxide (t-BuOK), the cross-coupling reaction between aryl fluorides and dimethyldisulfide was developed. A series of aryl methyl sulfides were obtained in moderate to good yields under transition-metal-free and mild conditions.

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