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85136-35-2

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85136-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85136-35-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,1,3 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 85136-35:
(7*8)+(6*5)+(5*1)+(4*3)+(3*6)+(2*3)+(1*5)=132
132 % 10 = 2
So 85136-35-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H30O2/c1-15(2,3)11-14(17)18-13-9-7-12(8-10-13)16(4,5)6/h12-13H,7-11H2,1-6H3

85136-35-2SDS

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 (4-tert-butylcyclohexyl) 3,3-dimethylbutanoate

1.2 Other means of identification

Product number -
Other names 4-(tert-Butyl)cyclohexyl 3,3-dimethylbutyrate

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:85136-35-2 SDS

85136-35-2Downstream Products

85136-35-2Relevant articles and documents

2-Norbornanediazonium Ions Revisited

Kirmse, Wolfgang,Siegfried, Rainer

, p. 950 - 956 (2007/10/02)

The reactions of 2-norbornanediazonium ions have been reinvestigated with the aid of optically active and deuterium-labeled precursors.Enantiomeric purities were determined by direct VPC methods, and deuterium distributions by 2H NMR spectroscopy.The product pattern is strongly affected by the polarity of the solvent. exo-Diazonium ions 13 in water yield racemic exo alcohol (s,kΔ) of the norbornadiazonium ions.Optically active exo products are typical of nonpolar solvents and originate most probably from assymetric ion pairs.Model studies with optically active bicyclooct-3-en-2-amine (36) provide conclusive evidence that ion-pair colapse may lead to optically active products even in the case of delocalized achiral carbocations.

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