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13905-48-1

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13905-48-1 Usage

General Description

1-Bromo-3-methylcyclohexane is a chemical compound with the molecular formula C7H13Br. It is a colorless liquid with a slightly sweet odor. The compound is commonly used in organic synthesis and as a reagent in chemical reactions. 1-Bromo-3-methylcyclohexane is mainly used in the production of pharmaceuticals and agrochemicals. It is also used as a solvent and in the manufacturing of specialty chemicals. The compound is considered to be potentially hazardous to human health if not handled and used properly, and precautions should be taken when working with it.

Check Digit Verification of cas no

The CAS Registry Mumber 13905-48-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,0 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13905-48:
(7*1)+(6*3)+(5*9)+(4*0)+(3*5)+(2*4)+(1*8)=101
101 % 10 = 1
So 13905-48-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H13Br/c1-6-3-2-4-7(8)5-6/h6-7H,2-5H2,1H3

13905-48-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-BROMO-3-METHYLCYCLOHEXANE

1.2 Other means of identification

Product number -
Other names Cyclohexane,1-bromo-3-methyl

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:13905-48-1 SDS

13905-48-1Relevant articles and documents

A CONVENIENT STEREOSPECIFIC ALKYLATION OF PHENYLACETYLENE BY ELECTROCHEMICAL REACTION OF ORGANOBORANES

Takahashi, Yuzuru,Tokuda, Masao,Itoh, Mitsuomi,Suzuki, Akira

, p. 461 - 464 (2007/10/02)

The electrochemical reaction of phenylacetylene with trialkylboranes in a tetrahydrofuran solution containing tetraalkylammonium halide gives the corresponding alkynes via a retention of configuration with respect to the boron-carbon bonds.The reaction mechanism is also discussed.

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