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36971-12-7

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36971-12-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36971-12-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,9,7 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 36971-12:
(7*3)+(6*6)+(5*9)+(4*7)+(3*1)+(2*1)+(1*2)=137
137 % 10 = 7
So 36971-12-7 is a valid CAS Registry Number.

36971-12-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-methylbut-3-en-2-yl)cyclohexan-1-ol

1.2 Other means of identification

Product number -
Other names 1-(1,1-Dimethyl-allyl)-cyclohexanol

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:36971-12-7 SDS

36971-12-7Relevant articles and documents

Rhodium catalysed carbonylation of homoallylic alcohols to spiropyrans bearing quaternary centres

Kitsos-Rzychon, Beate,Eilbracht, Peter

, p. 10721 - 10732 (1998)

A convenient preparation of substituted-spiropyrans via rhodium catalysed hydroformylation of homoallylic alcohols, followed by a condensation sequence to form hemiacetals and 2,2,3,3-tetraalkyl-4[H]- pyrans, is described.

Iron-catalyzed electrochemical allylation of carbonyl compounds by allylic acetates

Durandetti, Muriel,Meignein, Clotilde,Perichon, Jacques

, p. 3121 - 3124 (2007/10/03)

Homoallylic alcohols were synthesized from aldehydes or ketones and allylic acetates, using an electrochemical process catalyzed by iron complexes. We first studied the reactivity of allyl acetate, using N,N-dimethylformamide (DMF) or acetonitrile (AN) as solvent, FeBr2 as catalyst, and Fe as the sacrificial anode. Then we tested the regioreactivity of crotyl acetate and other allylic derivatives.

Indium mediated allylation and propargylation reactions of dimethyl acetals and ketals

Kwon, Jin Sun,Pae, Ae Nim,Choi, Kyung Il,Koh, Hun Yeong,Kim, Youseung,Cho, Yong Seo

, p. 1957 - 1959 (2007/10/03)

Indium mediated allylation and propargylation reactions of acetals and ketals with various allyl or propargyl bromides in aqueous media successfully provided the corresponding homoallylic or homopropargylic (and allenylic) alcohol, respectively, in moderate to good yields. Highly chemoselective allylation is also described. The ketal and aryl acetal could be selectively allylated over the aliphatic one in 80-84% yields.

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