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102910-30-5

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102910-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102910-30-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,9,1 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 102910-30:
(8*1)+(7*0)+(6*2)+(5*9)+(4*1)+(3*0)+(2*3)+(1*0)=75
75 % 10 = 5
So 102910-30-5 is a valid CAS Registry Number.

102910-30-5SDS

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 1,1,2,3,3-pentadeuterioprop-2-en-1-ol

1.2 Other means of identification

Product number -
Other names d5-allyl alcohol

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:102910-30-5 SDS

102910-30-5Relevant articles and documents

Synthesis of glycerol deuterated ether phospholipids

Nuss, Simone,Oudet, Pierre,Lebeau, Luc,Mioskowski, Charles

, p. 5705 - 5706 (1996)

1,3-Dialkyl glycerophosphocholines deuterated on the glycerol moiety were synthesized starting either from propiolic acid to yield a pentadeuterated compound, or from epibromohydrin to give a monodueterated substance.

Studies on thermal reactivity of β-(1,2-allenyl)butenolides and 2-allyl-3-allenylcyclohex-2-enones

Gu, Zhenhua,Ma, Shengming

experimental part, p. 2453 - 2464 (2009/04/10)

A series of thermal pericyclic reactions of β-allenylfuranones have been studied. It was observed that β-allenylfuranones would undergo 1,5-hydrogen shift to afford a new type of trienes upon heating. Due to their high reactivity, these trienes would undergo subsequent pericyclic reactions based on the nature of the substituent group R: When R is an alkyl group, the intermediate 4a or 4b would undergo a further 1,7-hydrogen shift to afford a more stable conjugated triene 3; with R being phenyl or cyclopropyl group, the 1,7-hydrogen shift was inhibited and the 4-type conjugated triene would form a six-membered ring 5 via 6π-electrocyclization. Interestingly, introducing another C=C double bond into the triene intermediate (R = CH=CH2), the 18-type intermediate would undergo 8π-electrocyclization reaction to form an eight-membered ring. Such a transformation was also observed with 2-allyl-3-allenylcyclohex-2-enones. The deuterium-labeling mechanistic studies show that the alkyl groups at the allenyl moiety of 1 participated in the isomerization process via 1,7-hydrogen shifts between 18 A, 20A, and 29 A.

Anwendung der Perdeuteroallyl Schutz-Gruppe

Thiem, Joachim,Mohn, Holger,Heesing, Albert

, p. 775 - 778 (2007/10/02)

Facile and straightforward transformations of propynoic acid into perdeuterated allyl bromide are described.The advantage of a pentadeuteroallyl protection for the 1H-N.M.R. structure elucidation of complex carbohydrate derivatives is demonstrated in the

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