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19214-95-0

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19214-95-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19214-95-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,1 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19214-95:
(7*1)+(6*9)+(5*2)+(4*1)+(3*4)+(2*9)+(1*5)=110
110 % 10 = 0
So 19214-95-0 is a valid CAS Registry Number.

19214-95-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,O-dideuterio-propan-2-ol

1.2 Other means of identification

Product number -
Other names O.2-Dideutero-propanol-(2)

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:19214-95-0 SDS

19214-95-0Upstream product

19214-95-0Relevant articles and documents

Combined Deuterium Nuclear Magnetic Resonance and Mass-spectrometric Studies of the Exchange Reactions of Ketones over Supported Metal Catalysts

Pope, Christopher,Kemball, Charles,McDougall, Gordon S.

, p. 747 - 752 (1990)

Deuterium NMR spectroscopy has been used in conjunction with mass spectrometry to study the exchange reaction of the ketones acetone, butan-2-one and cyclopentanone over a variety of supported metal catalysts.In many of the experiments simple, random, stepwise exchange was prevalent.However, in certain instances multiple exchange occurred.For butan-2-one and cyclopentanone this multiple exchange was essentially limited to the protons on carbon atoms adjacent ot the carbonyl group, while for acetone a strong preference towards exchange into only a single methyl groupwas noted.Some hydrogenation to propan-2-ol accompanied the multiple exchange of acetone, with the majority of the alcohol being formed by addition of D2 across the carbon oxygen double bond without simultaneous exchange into the methyl group, suggesting independent η1 and η2 adsorbed acetone surface intermediates for the exchange and hydrogenation reactions respectively.

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