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70553-75-2

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70553-75-2 Usage

Occurrence

An alkaloidal metabolite of Aspergillus flavus, this tremorgenic toxin is established from chemical degradations and spectroscopic data.

Check Digit Verification of cas no

The CAS Registry Mumber 70553-75-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,5,5 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 70553-75:
(7*7)+(6*0)+(5*5)+(4*5)+(3*3)+(2*7)+(1*5)=122
122 % 10 = 2
So 70553-75-2 is a valid CAS Registry Number.

70553-75-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name aflatrem

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:70553-75-2 SDS

70553-75-2Downstream Products

70553-75-2Relevant articles and documents

Nodulisporic acid e biosynthesis:: In vivo characterisation of NodD1, an indole-diterpene prenyltransferase that acts on an emindole SB derived indole-diterpene scaffold

Van De Bittner, Kyle C.,Cameron, Rosannah C.,Bustamante, Leyla Y.,Bundela, Rudranuj,Kessans, Sarah A.,Vorster, Jan,Nicholson, Matthew J.,Parker, Emily J.

, p. 1160 - 1164 (2019/07/25)

Prenylation of aromatic compounds is a key tailoring reaction in biosynthesis of bioactive indole-diterpenes. Here, we identify NodD1 as the enzyme responsible for the bisprenylation of nodulisporic acid F. This prenyltransferase showed a preference for its natural indole-diterpene substrate whereas other related enzymes were not able to catalyse this conversion.

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