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73723-49-6

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73723-49-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73723-49-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,7,2 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73723-49:
(7*7)+(6*3)+(5*7)+(4*2)+(3*3)+(2*4)+(1*9)=136
136 % 10 = 6
So 73723-49-6 is a valid CAS Registry Number.

73723-49-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dimethyl-3-(2-methylpropoxy)cyclohex-2-en-1-one

1.2 Other means of identification

Product number -
Other names 3-Isobutoxy-2,6-dimethylcyclohex-2-en-1-on

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:73723-49-6 SDS

73723-49-6Relevant articles and documents

Catalytic enantioselective approach to the eudesmane sesquiterpenoids: Total synthesis of (+)-carissone

Levine, Samantha R.,Krout, Michael R.,Stoltz, Brian M.

supporting information; experimental part, p. 289 - 292 (2009/08/08)

(Chemical Equation Presented) A catalytic enantioselective approach to the eudesmane sesquiterpenoids is reported. The strategic use of a palladium-catalyzed enantioselective alkylation of vinylogous ester substrates forged the C(10) all-carbon quaternary

Synthesis of β-chloro, β-bromo, and β-iodo α,β-unsaturated ketones

Piers, Edward,Grierson, John R.,Lau, Cheuk Kun,Nagakura, Isao

, p. 210 - 223 (2007/10/02)

A new, efficient method for the preparation of β-chloro, β-bromo, and β-iodo α,β-unsaturated ketones is described.The method involves the reaction of β-diketones or α-hydroxymethylenecycloalkanones with triphenylphosphine dihalides in the presence of trie

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