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144314-68-1

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144314-68-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144314-68-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,3,1 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 144314-68:
(8*1)+(7*4)+(6*4)+(5*3)+(4*1)+(3*4)+(2*6)+(1*8)=111
111 % 10 = 1
So 144314-68-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H21NO2/c1-11(2)5-4-6-12(3)7-8-13-9-14(15(17)18)16-10-13/h5,7,9-10,16H,4,6,8H2,1-3H3,(H,17,18)/b12-7+

144314-68-1SDS

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-[(2E)-3,7-dimethylocta-2,6-dienyl]-1H-pyrrole-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names EC 40

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:144314-68-1 SDS

144314-68-1Downstream Products

144314-68-1Relevant articles and documents

A brief total synthesis of Pyrrolostatin

Dunford, Damian G.,Knight, David W.

, p. 2746 - 2748 (2016)

A novel total synthesis of the unusual naturally occurring 2,4-disubstituted pyrrole, Pyrrolostatin 1, is described, which features formation of the central pyrrole ring by a recently developed silver(I)-catalysed 5-endo-dig cyclisation.

Short and highly efficient synthesis of lipid peroxidation inhibitor pyrrolostatin and some analogues thereof

Schmidt, Jens,Adrian, Juliane,Stark, Christian B.W.

, p. 8173 - 8176 (2015/08/03)

A highly efficient and scalable synthesis of potent lipid peroxidation inhibitor pyrrolostatin is reported (4 steps, 48%). In addition to the synthesis of the natural product, strategies for the preparation of analogues differing in the three structural subunits, the polar head group, the N-substituent and the lipophilic tail are described.

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