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19752-21-7

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19752-21-7 Usage

General Description

2-Methoxy-2-methylpropyl bromide is a chemical compound with the formula C5H11BrO. It is an ether and alkyl bromide, commonly used as an intermediate in organic synthesis. It is a clear, colorless liquid with a sweet odor and is insoluble in water but soluble in organic solvents. 2-METHOXY-2-METHYLPROPYL BROMIDE is commonly utilized in the production of pharmaceuticals, agrochemicals, and other specialty chemicals due to its reactivity and versatility. It is important to handle this chemical with caution, as it is harmful if swallowed or inhaled and can cause skin and eye irritation upon contact.

Check Digit Verification of cas no

The CAS Registry Mumber 19752-21-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,5 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19752-21:
(7*1)+(6*9)+(5*7)+(4*5)+(3*2)+(2*2)+(1*1)=127
127 % 10 = 7
So 19752-21-7 is a valid CAS Registry Number.

19752-21-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-2-methoxy-2-methylpropane

1.2 Other means of identification

Product number -
Other names 1-Brom-2-methyoxy-2-methyl-propan

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:19752-21-7 SDS

19752-21-7Downstream Products

19752-21-7Relevant articles and documents

Method for synthesis and 99m C labelling of 2-alkoxyisobutylisonitrile

-

, (2008/06/13)

A new method for synthesizing 2-alkoxyisobutylisonitrile is provided in which isobutylene is used as the starting material. The haloalkoxylation of isobutylene in alcohol medium gives 2-alkoxyisobutylhalide which is then converted to 2-alkoxyisobutylamine. In the basic condition, the reaction of 2-alkoxyisobutylamine with chloroform produces 2-alkoxyisobutylisonitrile. The synthesis process contains three steps by which a higher yield is achieved. 2-Alkoxyisobutylisonitrile is labelled with technetium-99m by exchange labelling of stable tetrakis(2-alkoxyisobutylisonitrile)copper(I) complex. Tetrakis(2-alkoxyisobutylisonitrile)copper(I) complex can be prepared by the exchange of acetonitrile molecules in tetrakis(acetonitrile)copper(I) complex with isonitrile ligands.

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