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252342-46-4

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252342-46-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 252342-46-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,2,3,4 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 252342-46:
(8*2)+(7*5)+(6*2)+(5*3)+(4*4)+(3*2)+(2*4)+(1*6)=114
114 % 10 = 4
So 252342-46-4 is a valid CAS Registry Number.

252342-46-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (5Z,13Z)-(2S,3R,4S,8S,9R,10R,11S,12S)-3,9-Bis-(tert-butyl-dimethyl-silanyloxy)-11-(4-methoxy-benzyloxy)-2,4,6,8,10,12-hexamethyl-hexadeca-5,13,15-trien-1-ol

1.2 Other means of identification

Product number -
Other names -

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:252342-46-4 SDS

252342-46-4Upstream product

252342-46-4Relevant articles and documents

Total synthesis and biological evaluation of a series of macrocyclic hybrids and analogues of the antimitotic natural products dictyostatin, discodermolide, and taxol

Paterson, Ian,Naylor, Guy J.,Gardner, Nicola M.,Guzman, Esther,Wright, Amy E.

scheme or table, p. 459 - 473 (2011/10/12)

The design, synthesis, and biological evaluation of a series of hybrids and analogues of the microtubule-stabilizing anticancer agents dictyostatin, discodermolide, and taxol is described. A 22-membered macrolide scaffold was prepared by adapting earlier

Development of a third-generation total synthesis of (+)-discodermolide: An expedient Still-Gennari-type fragment coupling utilizing an advanced β-ketophosphonate

Paterson, Ian,Lyothier, Isabelle

, p. 5494 - 5507 (2008/04/18)

A novel total synthesis of the complex polyketide discodermolide, a promising anticancer agent of marine sponge origin, has been completed in 11.1% overall yield over 21 linear steps. This third-generation approach features an unprecedented Still-Gennari-

Gram-scale synthesis of (+)-discodermolide.

Smith 3rd.,Kaufman,Beauchamp,LaMarche,Arimoto

, p. 1823 - 1826 (2008/02/11)

[formula: see text] A triply convergent, highly efficient second-generation synthesis of the potent antimitotic agent (+)-discodermolide (1) has been achieved on a 1-g scale.

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