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31138-32-6

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31138-32-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31138-32-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,1,3 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 31138-32:
(7*3)+(6*1)+(5*1)+(4*3)+(3*8)+(2*3)+(1*2)=76
76 % 10 = 6
So 31138-32-6 is a valid CAS Registry Number.

31138-32-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-6,10,14-trimethylpentadeca-9,13-dien-2-one

1.2 Other means of identification

Product number -
Other names (E)-6,10,14-trimethyl-pentadeca-9,13-dien-2-one

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:31138-32-6 SDS

31138-32-6Upstream product

31138-32-6Downstream Products

31138-32-6Relevant articles and documents

Diterpene Biosynthesis in Catenulispora acidiphila: On the Mechanism of Catenul-14-en-6-ol Synthase

Li, Geng,Guo, Yue-Wei,Dickschat, Jeroen S.

, p. 1488 - 1492 (2021)

A new diterpene synthase from the actinomycete Catenulispora acidiphila was identified and the structures of its products were elucidated, including the absolute configurations by an enantioselective deuteration approach. The mechanism of the cationic terpene cyclisation cascade was deeply studied through the use of isotopically labelled substrates and of substrate analogues with partially blocked reactivity, resulting in derailment products that gave further insights into the intermediates along the cascade. Their chemistry was studied, leading to the biomimetic synthesis of a diterpenoid analogue of a brominated sesquiterpene known from the red seaweed Laurencia microcladia.

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