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73428-04-3

73428-04-3

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73428-04-3 Usage

Chemical Properties

Yellow Crystalline Solid

Uses

A photocleavable protecting group for carboxylic acids

Check Digit Verification of cas no

The CAS Registry Mumber 73428-04-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,4,2 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 73428-04:
(7*7)+(6*3)+(5*4)+(4*2)+(3*8)+(2*0)+(1*4)=123
123 % 10 = 3
So 73428-04-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO3/c13-7-10-5-8-3-1-2-4-9(8)6-11(10)12(14)15/h1-6,13H,7H2

73428-04-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-nitronaphthalen-2-yl)methanol

1.2 Other means of identification

Product number -
Other names 3-nitro-2-napthalenemethanol

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:73428-04-3 SDS

73428-04-3Relevant articles and documents

NUCLEIC ACID BINDING COMPOUNDS, METHODS OF MAKING, AND USE THEREOF

-

Page/Page column 46-47, (2012/07/14)

The present invention relates to oligomer compounds, including dimers and trimers, formed by a disulfide, sulfinyl thio, olefin or hydrocarbon bond, or a hydrazone exchange bond between two or more monomers. Methods of making the monomers and the oligomers is also disclosed. Use of the compounds for inhibiting the activity of target RNA molecules, particularly those having a secondary structure that include a stem or stem-loop formation. Dimer compounds capable of inhibiting the activity of an HIV-1 RNA frameshifting stem-loop and a (CUG)n expanded repeat stem- loop are disclosed, as are methods of treating diseases associated with these target RNA molecules.

Plant antitumor agents: Synthesis and biological activity of camptothecin analogues

Wani,Ronman,Lindley,Wall

, p. 554 - 560 (2007/10/02)

Four analogues, 10-methoxy (20), 12-aza (29), benz[j] (36), and 18-methoxy (38), of camptothecin were obtained by total synthesis. The two water-soluble analogues, 10-[(carboxymethyl)oxy] (24) and 10-[2'-(diethylamino)-ethoxy]-20(S)-camptothecin (26), wit

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