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105041-68-7

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105041-68-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105041-68-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,0,4 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 105041-68:
(8*1)+(7*0)+(6*5)+(5*0)+(4*4)+(3*1)+(2*6)+(1*8)=77
77 % 10 = 7
So 105041-68-7 is a valid CAS Registry Number.

105041-68-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-isopropyl-3-methoxybenzonitrile

1.2 Other means of identification

Product number -
Other names .3-Methoxy-2-isopropyl-benzoesaeure-nitril

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:105041-68-7 SDS

105041-68-7Relevant articles and documents

The synthesis and antimicrobial activity of heterocyclic derivatives of totarol

Kim, Michelle B.,O'Brien, Terrence E.,Moore, Jared T.,Anderson, David E.,Ames, James B.,Shaw, Jared T.,Foss, Marie H.,Weibel, Douglas B.

supporting information, p. 818 - 822,5 (2012/12/12)

The synthesis and antimicrobial activity of heterocyclic analogues of the diterpenoid totarol are described. An advanced synthetic intermediate with a ketone on the A-ring is used to attach fused heterocycles, and a carbon-to-nitrogen atom replacement is made on the B-ring by de novo synthesis. A-ring analogues with an indole attached exhibit, for the first time, enhanced antimicrobial activity relative to the parent natural product. Preliminary experiments demonstrate that the indole analogues do not target the bacterial cell division protein FtsZ as had been hypothesized for totarol.

Synthesis of antimicrobial natural products targeting FtsZ: (+)-totarol and related totarane diterpenes

Kim, Michelle B.,Shaw, Jared T.

supporting information; experimental part, p. 3324 - 3327 (2010/11/02)

(Equation Presented). An efficient, convergent synthesis of totarol by a diastereoselective epoxide/alkene/arene bicyclization is described. The reported synthesis enables the preparation of related diterpenes totaradiol and totarolone as well as previously unavailable derivatives that exhibit comparable inhibition of the bacterial cell division protein FtsZ.

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