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22094-18-4

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22094-18-4 Usage

Chemical Properties

white crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 22094-18-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,9 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 22094-18:
(7*2)+(6*2)+(5*0)+(4*9)+(3*4)+(2*1)+(1*8)=84
84 % 10 = 4
So 22094-18-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H10Br2O2/c1-8-5(3-6,4-7)9-2/h3-4H2,1-2H3

22094-18-4 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (A11217)  1,3-Dibromo-2,2-dimethoxypropane, 99%   

  • 22094-18-4

  • 5g

  • 853.0CNY

  • Detail
  • Alfa Aesar

  • (A11217)  1,3-Dibromo-2,2-dimethoxypropane, 99%   

  • 22094-18-4

  • 25g

  • 3628.0CNY

  • Detail
  • Alfa Aesar

  • (A11217)  1,3-Dibromo-2,2-dimethoxypropane, 99%   

  • 22094-18-4

  • 100g

  • 7382.0CNY

  • Detail

22094-18-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-Dibromo-2,2-dimethoxypropane

1.2 Other means of identification

Product number -
Other names 1,3-Dibrom-aceton-dimethylacetal

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:22094-18-4 SDS

22094-18-4Relevant articles and documents

Chlorination of Aliphatic Ketones in Methanol

Gallucci, R. R.,Going, R.

, p. 2532 - 2538 (2007/10/02)

The chlorination of aliphatic ketones in methanol has been examined.The product distributions in methanol differ substantially from those obtained by chlorination in carbon tetrachloride.The reaction in methanol favors addition of chlorine to the least substituted carbon α to the carbonyl group.The effect is especially pronounced if an α carbon bearing two substituents is present.The distribution of products is determined by the relative stability of the enol ethers formed from the ketone under the reaction conditions.

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