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34723-82-5

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34723-82-5 Usage

Chemical Properties

Colorless to yellow liquid

Uses

2-(Bromomethyl)tetrahydro-2H-pyran has been used in the preparation of tellurated heterocycles, 2-[(2-thienyltelluro)methyl]tetrahydrofuran and [(2-thienyltelluro)methyl]tetrahydro-2H-pyran.

General Description

Cross-coupling reaction of 2-(bromomethyl)tetrahydro-2H-pyran with potassium heteroaryltrifluoroborates has been investigated.

Check Digit Verification of cas no

The CAS Registry Mumber 34723-82-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,7,2 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 34723-82:
(7*3)+(6*4)+(5*7)+(4*2)+(3*3)+(2*8)+(1*2)=115
115 % 10 = 5
So 34723-82-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H11BrO/c7-5-6-3-1-2-4-8-6/h6H,1-5H2

34723-82-5 Well-known Company Product Price

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  • Aldrich

  • (262579)  2-(Bromomethyl)tetrahydro-2H-pyran  98%

  • 34723-82-5

  • 262579-5G

  • 1,301.04CNY

  • Detail
  • Aldrich

  • (262579)  2-(Bromomethyl)tetrahydro-2H-pyran  98%

  • 34723-82-5

  • 262579-25G

  • 5,009.94CNY

  • Detail

34723-82-5SDS

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 2-(bromomethyl)oxane

1.2 Other means of identification

Product number -
Other names Tetrahydro-2H-pyran-2-methyl bromide

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:34723-82-5 SDS

34723-82-5Upstream product

34723-82-5Relevant articles and documents

A new simple and industrial process for bromination of alcohols

Mas,Metivier

, p. 2187 - 2191 (2007/10/02)

Alcohols treated with thionylchloride, followed by chlorine/bromine exchange using gaseous hydrobromic acid and thermal decomposition in the presence of a tertiary amine give the corresponding brominated compounds. The process is regio/stereo selective.

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