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1438-65-9

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1438-65-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1438-65-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,3 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1438-65:
(6*1)+(5*4)+(4*3)+(3*8)+(2*6)+(1*5)=79
79 % 10 = 9
So 1438-65-9 is a valid CAS Registry Number.

1438-65-9SDS

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 5-[5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-1-en-3-ol

1.2 Other means of identification

Product number -
Other names Labda-8(20),14-diene-13,19-diol

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:1438-65-9 SDS

1438-65-9Upstream product

1438-65-9Downstream Products

1438-65-9Relevant articles and documents

Microbial Transformation of Manool and (12Z)-Labda-8(17),12,14-triene by Rhodococcus erythropolis JTS-131

Hieda, Tadaharu,Mikami, Yoichi,Obi, Yukiteru

, p. 787 - 794 (2007/10/02)

Rhodococcus erythropolis JTS-131, a cis-abienol and sclareol transformable bacterium, converted manool and accumulated manoyl oxide in the culture broth.In the presence of metabolic inhibitors, 13β-hydroxylabda-8(17),14-dien-18-oic acid and its methylester (a new compound) were accumulated as the transformation products.This strain also transformed (12Z)-labda-8(17),12,14-triene and accumulated (12Z)-labda-8(17),12,14-trien-18-al in the culture broth.In the presence of metabolic inhibitors, two compounds, (12Z)-labda-8(17),12,14-trien-18-ol and 4,18,19-trinor-3,4-seco-5-oxo-(12Z)-labda-8(17),12,14-trien-3-oic acid were accumulated.Based on the experiments on the degradation sequence, transformation pathways for these two labdanes by the bacterium are proposed.

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