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6353-54-4

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6353-54-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6353-54-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,5 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6353-54:
(6*6)+(5*3)+(4*5)+(3*3)+(2*5)+(1*4)=94
94 % 10 = 4
So 6353-54-4 is a valid CAS Registry Number.

6353-54-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-tert-butyl-1-methylcyclohexan-1-ol

1.2 Other means of identification

Product number -
Other names cis-4-tert-Butyl-1-propoxycyclohexan

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:6353-54-4 SDS

6353-54-4Relevant articles and documents

Ambergris and/or indole-like compositions of odoriferous substances

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Page/Page column 17, (2021/02/17)

The present invention primarily relates to the use of one or more compound(s) of formula (I) as fragrance, wherein R is methyl or ethyl and R1 is H, methyl or ethyl. The invention further relates to new fragrance compositions comprising one or

Tandem application of C-C bond-forming reactions with reductive ozonolysis

Willand-Charnley, Rachel,Dussault, Patrick H.

, p. 42 - 47 (2013/03/29)

Several variants of reductive ozonolysis, defined here as the in situ generation of aldehydes or ketones during ozonolytic cleavage of alkenes, are demonstrated to work effectively in tandem with a number of C-C bond-forming reactions. For reactions involving basic nucleophiles (1,2- addition of Grignard reagents, Wittig or Horner-Emmons olefinations, and directed aldol reactions of lithium enolates), the one-pot process offers a rapid and high-yielding alternative to traditional two-step protocols.

Ketone coupling with alkyl iodides, bromides, and chlorides using thulium diiodide: A more powerful version of SmI2(THF)(x)/HMPA

Evans, William J.,Allen, Nathan T.

, p. 2118 - 2119 (2007/10/03)

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