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136539-81-6

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136539-81-6 Usage

Physical state

Colorless liquid.

Odor

Strong and disagreeable.

Classification

Bromoalkane.

Uses

Intermediate in organic synthesis, production of pharmaceuticals and agrochemicals, solvent in organic reactions, and reagent in chemical research.

Hazardous nature

Potential health risks associated with ingestion, inhalation, and skin contact.

Safety measures

Handle with caution and proper safety measures.

Check Digit Verification of cas no

The CAS Registry Mumber 136539-81-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,5,3 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 136539-81:
(8*1)+(7*3)+(6*6)+(5*5)+(4*3)+(3*9)+(2*8)+(1*1)=146
146 % 10 = 6
So 136539-81-6 is a valid CAS Registry Number.

136539-81-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-BROMO-7-METHYLNONANE

1.2 Other means of identification

Product number -
Other names 7-methyl-1-bromononane

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:136539-81-6 SDS

136539-81-6Relevant articles and documents

Studies related to fatty acid desaturation. Part I: Preparation of methyl-substituted nonanols, nonyl bromides and total synthesis of new branched oleic acids

Genard, S.,Patin, H.

, p. 397 - 406 (2007/10/02)

Convenient pathways for the synthesis of seven structurally defined isomers of methyl-nonanols and methyl-nonylbromides are described.These synthons are used to perform Wittig reactions between convenient phosphoranes and aldehydes in order to obtain seven new octadecenoic acids bearing a methyl grouping on carbons 11 to 17. branched nonan-1-ols / branched 1-nonylbromides / Wittig reactions / methyl 9-bromononanoate / methyl 8-formyloctanoate / methyl 11 or 17-methyloctadec-9-enoates

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