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101110-74-1

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101110-74-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101110-74-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,1,1 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 101110-74:
(8*1)+(7*0)+(6*1)+(5*1)+(4*1)+(3*0)+(2*7)+(1*4)=41
41 % 10 = 1
So 101110-74-1 is a valid CAS Registry Number.

101110-74-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-(5'-formyl-2'-methoxyphenoxy)benzoate

1.2 Other means of identification

Product number -
Other names 4-(5-Formyl-2-methoxy-phenoxy)-benzoesaeure-methylester

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:101110-74-1 SDS

101110-74-1Relevant articles and documents

SYNTHESIS AND STRUCTURE CONFIRMATION OF RICCARDIN B, A MACROCYCLIC BIS(BIBENZYL) FROM THE LIVERWORT, RICCARDIA MULTIFIDA

Shiobara, Yoshinori,Sumitomo, Hisako,Tsukamoto, Michiyo,Harada, Chiemi,Kodama, Mitsuaki

, p. 1587 - 1588 (1985)

Riccardin B, a cytotoxic bis(bibenzyl) obtained from a liverwort was synthesized via an intramolecular Wittig-type reaction and the structure was established unequivocally.

Design, synthesis, biological evaluation and molecular modeling study of novel macrocyclic bisbibenzyl analogues as antitubulin agents

Sun, Bin,Li, Lin,Hu, Qing-wen,Zheng, Hong-bo,Tang, Hui,Niu, Huan-min,Yuan, Hui-qing,Lou, Hong-xiang

, p. 186 - 208 (2017/02/26)

A series of macrocyclic bisbibenzyls with novel skeletons was designed, synthesized, and evaluated for antiproliferative activity against five anthropic cancer cell lines. Among these novel molecules, compound 47 displayed excellent anticancer activity ag

Bisbibenzyl derivatives sensitize vincristine-resistant KB/VCR cells to chemotherapeutic agents by retarding P-gp activity

Xi, Guang-Min,Sun, Bin,Jiang, Hui-Hui,Kong, Feng,Yuan, Hui-Qing,Lou, Hong-Xiang

experimental part, p. 6725 - 6733 (2010/10/19)

P-glycoprotein (P-gp) is known to mediate multidrug resistance (MDR) by acting as an efflux pump to actively transport chemotherapeutic agents out of carcinoma cells. Inhibition of P-gp function may represent one of the strategies to reverse MDR. We have

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