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2875-95-8

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2875-95-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2875-95-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,7 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2875-95:
(6*2)+(5*8)+(4*7)+(3*5)+(2*9)+(1*5)=118
118 % 10 = 8
So 2875-95-8 is a valid CAS Registry Number.
InChI:InChI=1S/C3H8/c1-3-2/h3H2,1-2H3/i3D2

2875-95-8 Well-known Company Product Price

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  • Aldrich

  • (493317)  Propane-2,2-d2  98 atom % D

  • 2875-95-8

  • 493317-1L-EU

  • 11,196.90CNY

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2875-95-8SDS

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 2,2-dideuteriopropane

1.2 Other means of identification

Product number -
Other names Propane-2,2-d2

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:2875-95-8 SDS

2875-95-8Relevant articles and documents

Steiner et al.

, p. 189,200 (1961)

Unprecedented double nucleophilic addition of a hydride at a central carbon of an η3-allyl ligand

Minato, Makoto,Sekimizu, Ryoko,Uchida, Daisuke,Ito, Takashi

, p. 3695 - 3698 (2004)

Treatment of η3-allyl compound [Cp 2Mo(η3-C3H5)]+ (1; Cp = η5-C5H5) with MH (M = Li, Na) resulted in reduction of the allyl ligand to give propane. Deuterium-labeling studies were used to trace the origins and fates of the hydrogen atoms. The mechanism is discussed in light of the HSAB principle. The studies showed that the formation of propane can be explained by 1,2-hydrogen migration from the central to the terminal carbon of the allyl ligand, and the subsequent double nucleophilic addition of the hydride at the central carbon.

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