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7-methoxy-5-nitro-1-benzofuran-2-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25672-29-1

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25672-29-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25672-29-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,6,7 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 25672-29:
(7*2)+(6*5)+(5*6)+(4*7)+(3*2)+(2*2)+(1*9)=121
121 % 10 = 1
So 25672-29-1 is a valid CAS Registry Number.

25672-29-1SDS

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 7-methoxy-5-nitro-1-benzofuran-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 7-methoxy-5-nitro-benzofuran-2-carboxylic 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:25672-29-1 SDS

25672-29-1Relevant academic research and scientific papers

Total synthesis of seco (+)- and ent-(-)-oxaduocarmycin SA: Construction of the (chloromethyl)indoline alkylating subunit by a novel intramolecular aryl radical cyclization onto a vinyl chloride

Patel, Vinod F.,Andis, Sherri L.,Enkema, Julia K.,Johnson, David A.,Kennedy, Joseph H.,Mohamadi, Fariborz,Schultz, Richard M.,Soose, Daniel J.,Spees, Michael M.

, p. 8868 - 8874 (1997)

A practical, total synthesis of seco-(+)-oxaduocarmycin 3a, an analogue of the highly cytotoxic natural product, duocarmycin SA (1), is described. the 13-step synthesis feature a novel and efficient intramolecular aryl radical cyclization onto a vinyl chloride as a direct entry to the (chloromethyl)indoline alkylating subunit 14. Subsequent resolution, utilizing a preparative Chiralpak AD column, provided enantiomerically pure alkylating subunits 14a and 14b which were elaborated to seco-(+) and ent-(- )-oxduocarmycins, 3a and 3b. respectively. The natural enantiomer 3a was active at pM concentrations and exhibited 7-50-fold higher potentcy than its enantiomer 3b in in vitro cytotoxicity assays.

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