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918902-48-4

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918902-48-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 918902-48-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,8,9,0 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 918902-48:
(8*9)+(7*1)+(6*8)+(5*9)+(4*0)+(3*2)+(2*4)+(1*8)=194
194 % 10 = 4
So 918902-48-4 is a valid CAS Registry Number.

918902-48-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Boc-Trp(Boc)-Phe methyl ester

1.2 Other means of identification

Product number -
Other names Boc-Trp(Boc)-Phe-OMe

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:918902-48-4 SDS

918902-48-4Relevant articles and documents

A Mutasynthesis Approach with a Penicillium chrysogenum ΔroqA Strain Yields New Roquefortine D Analogues

Ouchaou, Kahina,Maire, Florian,Salo, Oleksandr,Ali, Hazrat,Hankemeier, Thomas,Van Der Marel, Gijsbert A.,Filippov, Dmitri V.,Bovenberg, Roel A. L.,Vreeken, Rob J.,Driessen, Arnold J. M.,Overkleeft, Herman S.

, p. 915 - 923 (2015/04/14)

Penicillium chrysogenum, which lacks the roqA gene, processes synthetic, exogenously added histidyltryptophanyldiketopiperazine (HTD) to yield a set of roquefortine-based secondary metabolites also produced by the wild-type strain. Feeding a number of synthetic HTD analogues to the ΔroqA strain gives rise to the biosynthesis of a number of new roquefortine D derivatives, depending on the nature of the synthetic HTD added. Besides delivering semisynthetic roquefortine analogues, the mutasynthesis studies presented here also shed light on the substrate preferences and molecular mechanisms employed by the roquefortine C/D biosynthesis gene cluster, knowledge that may be tapped for the future development of more complex semisynthetic roquefortine-based secondary metabolites.

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