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81520-10-7

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81520-10-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81520-10-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,2 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 81520-10:
(7*8)+(6*1)+(5*5)+(4*2)+(3*0)+(2*1)+(1*0)=97
97 % 10 = 7
So 81520-10-7 is a valid CAS Registry Number.

81520-10-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3S,4S)-5-Benzyloxy-2,4-dimethylpentan-1,3-diol

1.2 Other means of identification

Product number -
Other names -

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:81520-10-7 SDS

81520-10-7Relevant articles and documents

Synthesis of polypropionate subunits from cyclopropanes

Defosseux, Magali,Blanchard, Nicolas,Meyer, Christophe,Cossy, Janine

, p. 7632 - 7653 (2007/10/03)

The oxymercuration-reductive demercuration of several cyclopropanealkanol or their derivatives bearing adjacent stereocenters has been investigated in order to synthesize polypropionate subunits. The crucial importance of the ester protecting group for th

Synthesis of stereotriads by oxymercuration of substituted cyclopropylcarbinols.

Cossy,Blanchard,Meyer

, p. 2567 - 2569 (2007/10/03)

[structure: see text] Cyclopropylcarbinol derivatives bearing an adjacent methyl-substituted stereocenter and a remote beta-hydroxy group protected as a pivalate underwent anchimerically assisted regio- and diastereoselective oxymercurations, affording af

Stereoselective Total Synthesis of (+/-)-Invictolide. An Efficient Preparation of a Trisubstituted δ-Lactone from Aldol Precursors

Pilli, Ronaldo Aloise,Murta, Maria Marcia

, p. 338 - 342 (2007/10/02)

The stereoselective total synthesis of (+/-)-invictolide (1), a component of the queen recognition pheromone of Solenopsis invicta, is described.The TiCl4-mediated addition of silyl ketene thioacetal 8 to (+/-)-3-(benzyloxy)-2-methylpropionaldehyde afford

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