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1072901-59-7

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  • 3-[(9-Fluorenylmethoxycarbonyl)amino]-p-toluic acid;3-[(9-Fluorenylmethoxycarbonyl)amino]-4-methylbenzoic acid

    Cas No: 1072901-59-7

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1072901-59-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1072901-59-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,2,9,0 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1072901-59:
(9*1)+(8*0)+(7*7)+(6*2)+(5*9)+(4*0)+(3*1)+(2*5)+(1*9)=137
137 % 10 = 7
So 1072901-59-7 is a valid CAS Registry Number.

1072901-59-7SDS

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 3-(9H-fluoren-9-ylmethoxycarbonylamino)-4-methylbenzoic acid

1.2 Other means of identification

Product number -
Other names 3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-methylbenzoic 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:1072901-59-7 SDS

1072901-59-7Downstream Products

1072901-59-7Relevant articles and documents

New antimitotic agents with activity in multi-drug-resistant cell lines and in vivo efficacy in murine tumor models

Szczepankiewicz,Chiou,Credo,Alder,Nukkala,Zielinski,Jarvis,Mollison,Frost,Bauch,Hui,Liu,Claiborne,Li,Rosenberg,Jae,Tasker,Gunawardana,Von Geldern,Gwaltney II,Wu-Wong,Gehrke

, p. 4416 - 4430 (2007/10/03)

During a screen for compounds that could inhibit cell proliferation, a series of new tubulin-binding compounds was identified with the discovery of oxadiazoline 1 (A-105972). This compound showed good cytotoxic activity against non-multi-drug-resistant and multi-drug-resistant cancer cell lines, but its utility in vivo was limited by a short half-life. Medicinal chemistry efforts led to the discovery of indolyloxazoline 22g (A-259745), which maintained all of the in vitro activity seen with oxadiazoline 1, but also demonstrated a better pharmacokinetic profile, and dose-dependent in vivo activity. Over a 28 day study, indolyloxazoline 22g increased the life span of tumor-implanted mice by up to a factor of 3 upon oral dosing. This compound, and others of its structural class, may prove to be useful in the development of new chemotherapeutic agents to treat human cancers.

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