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26675-10-5

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26675-10-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26675-10-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,6,7 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 26675-10:
(7*2)+(6*6)+(5*6)+(4*7)+(3*5)+(2*1)+(1*0)=125
125 % 10 = 5
So 26675-10-5 is a valid CAS Registry Number.

26675-10-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4a-methyl-3,4,5,6,7,8-hexahydro-2H-naphthalen-2-ol

1.2 Other means of identification

Product number -
Other names 4a-methyl-2,3,4,4a,5,6,7,8-octahydronaphthalen-2-ol

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:26675-10-5 SDS

26675-10-5Relevant articles and documents

Steric and complexation effects on the 1,4-addition reaction of lithium dimethylcuprate with rigid α,β-unsaturated ketones

Vellekoop, A. Samuel,Smith, Robin A.J.

, p. 11971 - 11994 (2007/10/03)

Reaction of lithium dimethylcuprate with a series of substituted 10- methyl-l(9)-octal-2-ones in diethyl ether give 1,4-addition products with the same ring junction stereochemistry as the parent, unsubstituted α,β- unsaturated ketone. The reactivity of the system is modified by groups positioned axially and 1,3 with respect to the β-carbon of the enone. Alkoxy substituents are generally activating, particularly if they are syn with respect to the incoming methyl group.

SELECTIVITE DE LA REDUCTION D'α-ENONES POLYCYCLIQUES PAR LES BOROHYDRURES: EFFET DE L'ADDITION DE TETRAMETHYL-ETHYLENEDIAMINE AU BOROHYDRURE DE TETRABUTYLAMMONIUM

D'incan, E.,Loupy, A.,Maia, A.,Seyden-Penne, J.,Viout, P.

, p. 2923 - 2927 (2007/10/02)

Δ1,9octalone, Δ1,9-10-methyl octalone and testosterone were reduced by NBu4BH4, alone or in the presence of tetramethylethylenediamine (TMEDA), in THF and in toluene.With TMEDA, the first step of the reduction is the regioselective 1,4 attack by BH4(1-) which leads either to the saturated ketones or to the corresponding saturated alcohols.The results observed under different conditions were interpreted by the intervention of various reductive species: diborane, enoxyborohydrides in the absence of TMEDA, amine-borane in its presence.

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