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Benzeneacetic acid, 5-formyl-3-methoxy-2-(methoxycarbonyl)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

137787-62-3

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137787-62-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137787-62-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,7,8 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 137787-62:
(8*1)+(7*3)+(6*7)+(5*7)+(4*8)+(3*7)+(2*6)+(1*2)=173
173 % 10 = 3
So 137787-62-3 is a valid CAS Registry Number.

137787-62-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl-5-formyl-3-methoxyhomophthalate

1.2 Other means of identification

Product number -
Other names 4-Formyl-2-methoxy-6-methoxycarbonylmethyl-benzoic acid methyl ester

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:137787-62-3 SDS

137787-62-3Relevant academic research and scientific papers

Total Synthesis of Novel Xanthone Antibiotics (+/-)-Cervinomycins A1 and A2

Mehta, Goverdhan,Shah, Shailesh R.,Venkateswarlu, Yenamandra

, p. 11729 - 11742 (2007/10/02)

A total synthesis of novel heptacyclic antibiotics cervinomycin A1 1 and A2 2 following a convergent approach is reported.The cornerstone of our strategy was the construction of the central ring D through photochemical electrocyclization.The oxazolo-isoquinoline fragment (ABC rings) 7 and the xanthone fragment (EFG rings) 8 were assembled through relatively straightforward synthetic protocols and coupled through a Wittig reaction to give 6 and set up the key photocyclization.Our successful approach to 1 and 2 can be readily adapted to the synthesis of analogues of these interesting antibiotics.

Total Synthesis of Cervinomycin A1-trimethyl Ether and Cervinomycin A2-methyl Ether

Mehta, Goverdhan,Shah, Shailesh R.

, p. 5195 - 5198 (2007/10/02)

The heptacyclic framework of cervinomycin antibiotics has been constructed through a C+EFG -> CEFG -> CDEFG -> ABCDEFG approach in which the photochemical generation of ring D was a key step.Key words: Xanthone antibiotics, Photocyclisation, Tetrahydrooxazolobenzisoquinolone formation.

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