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100612-88-2

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100612-88-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100612-88-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,6,1 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 100612-88:
(8*1)+(7*0)+(6*0)+(5*6)+(4*1)+(3*2)+(2*8)+(1*8)=72
72 % 10 = 2
So 100612-88-2 is a valid CAS Registry Number.

100612-88-2SDS

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 1-(5-(allyloxy)-2,4-dimethoxyphenyl)ethanone

1.2 Other means of identification

Product number -
Other names 5-Allyloxy-2,4-dimethoxyacetophenone

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:100612-88-2 SDS

100612-88-2Relevant articles and documents

Towards an asymmetric synthesis of the bacterial peptide deformylase (PDF) inhibitor fumimycin

Hartmann, Caroline E.,Gross, Patrick J.,Nieger, Martin,Braese, Stefan

supporting information; experimental part, p. 5059 - 5062 (2010/04/04)

Studies towards the synthesis of the bacterial peptide deformylase (PDF) inhibitor fumimycin are reported. The synthetic approach features an organocatalytic access to the α,α-disubstituted amino acid unit and results in the synthesis of an advanced inter

Syntheses of isochromane analogues of the michellamines and korupensamines

De Koning, Charles B.,Michael, Joseph P.,Van Otterlo, Willem A.L.

, p. 799 - 811 (2007/10/03)

Syntheses of the oxygen analogues 6, 7 and 8 of the michellamines 1 and korupensamines 2 are described. Racemic 5-iodo-6,8-dimethoxy-trans-1,3-dimethylisochromane 10 was synthesised in eleven steps from 2,4-dimethoxybenzaldehyde in an overall yield of 51%

An investigation into the electronic effects of substituents at the 6-position on the biological activity of isochromanquinones

Green, Ivan R.,De Koning, Charles B.,Hugo, Victor I.

, p. 112 - 119 (2007/10/03)

Three isochromanquinones 10, 11 and 12 were synthesised in order to determine the effect of electronic effects of groups at the 6-position on the biological activity of these compounds.

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