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37931-65-0

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37931-65-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37931-65-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,9,3 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 37931-65:
(7*3)+(6*7)+(5*9)+(4*3)+(3*1)+(2*6)+(1*5)=140
140 % 10 = 0
So 37931-65-0 is a valid CAS Registry Number.

37931-65-0SDS

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 methyl 6-methoxy-1,4a-dimethyl-9-oxo-3,4-dihydro-2H-phenanthrene-1-carboxylate

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:37931-65-0 SDS

37931-65-0Downstream Products

37931-65-0Relevant articles and documents

Reactions of podocarpic acid derivatives with thallium(III) nitrate

Miles,Lho,Chittawong,Payne

, p. 4034 - 4036 (2007/10/02)

The reaction of methyl O-methyl-7-ketopodocarpate (3) with thallium(III) nitrate in acetic acid was performed in attempt to synthesize compound 4, an intermediate in the total synthesis of the plant growth hormone gibberellic acid. The reaction unexpectedly resulted in new methodology for the one-step formation of methyl O-methyl-Δ5,6-7-ketopodocarpate from the keto ester 3. Four model compounds, having similar skeletons to the keto ester 3, were reacted with TTN under the same conditions to establish a general method for the formation of α,β-unsaturated ketones. These models yielded either the α-nitrato ketone and/or the decomposition product benzoic acid. Reaction of the hindered tricyclic ketone 11 with TTN yielded the expected α,β-unsaturated ketone 12. Thus this methodology is selective for hindered tricyclic ketone systems.

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