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6931-71-1

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6931-71-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6931-71-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,3 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6931-71:
(6*6)+(5*9)+(4*3)+(3*1)+(2*7)+(1*1)=111
111 % 10 = 1
So 6931-71-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H22O2/c1-5-9(11,6-2)10(12,7-3)8-4/h11-12H,5-8H2,1-4H3

6931-71-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-diethylhexane-3,4-diol

1.2 Other means of identification

Product number -
Other names 3,4-Hexanediol, 3,4-diethyl-

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:6931-71-1 SDS

6931-71-1Relevant articles and documents

Sml2-promoted reformatsky-type reaction and acylation of alkyl 1-chlorocyclopropanecarboxylates

Nagano, Takao,Motoyoshiya, Jiro,Kakehi, Akikazu,Nishii, Yoshinori

supporting information; experimental part, p. 5453 - 5456 (2009/06/28)

(Chemical Equation Presented) In the presence of HMPA in THF, highly stereoselective Sml2-promoted substitutions of alkyl 1-chlorocyclopropanecarboxylates 1 using various ketones, aldehydes (Reformatsky-type reaction), and acyl chlorides (acyla

New insights into the mechanism of the McMurry reaction

Villiers, Claude,Ephritikhine, Michel

, p. 2380 - 2382 (2007/10/03)

-

TiCl4/Mg/BrCH2CH2Br Reagent System: A 1,2-Diorganometallic Equivalent

Rao, S. Achyutha,Periasamy, M.

, p. 1583 - 1586 (2007/10/02)

1,2-Diorganometallic species generated utilizing the TiCl4/Mg/BrCH2CH2/Br reagent system reacts with ketones to give the corresponding 1,4-diols and/or 1,2-diols in moderate yields.

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