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135082-42-7

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135082-42-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135082-42-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,0,8 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 135082-42:
(8*1)+(7*3)+(6*5)+(5*0)+(4*8)+(3*2)+(2*4)+(1*2)=107
107 % 10 = 7
So 135082-42-7 is a valid CAS Registry Number.

135082-42-7SDS

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 4-(benzyloxy)-3-methoxy-N-(2,3,4,5-tetramethoxyphenyl)anthranilic acid

1.2 Other means of identification

Product number -
Other names 4-benzyloxy-3-methoxy-N-(2,3,4,5-tetramethoxyphenyl) anthranilic acid

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:135082-42-7 SDS

135082-42-7Relevant articles and documents

SYNTHESIS OF GLYFOLINE, A CONSTITUENT OF GLYCOSMIS CITRIFOLIA (WILLD.) LINDL. AND A POTENTIAL ANTICANCER AGENT

Su, Tsann-Long,Dziewiszek, Krzysztof,Wu, Tian-Shung

, p. 1541 - 1544 (1991)

Condensation of 4-benzyloxy-3-methoxyanthranilic acid (3) with 5-iodo-1,2,3,4-tetramethoxybenzene (4) gave 6-benzyloxy-1,2,3,4,5-pentamethoxy-9-acridone (7), which was then converted into glyfoline (1) via N-methylation, selective de-O-methylation, and de

Synthesis of the acridone alkaloids glyfoline and congeners. Structure- activity relationship studies of cytotoxic acridones

Su,Kohler,Chou,Moon Woo Chun,Watanabe

, p. 2703 - 2710 (2007/10/02)

Glyfoline (4, 1,6-dihydroxy-10-methyl-2,3,4,5-tetramethoxyacridin-9-one) and its congeners were synthesized for evaluation of their cytotoxicity. A detailed structure-activity relationships (SAR) of these acridone derivatives were also studied. To study t

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