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65907-71-3

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65907-71-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65907-71-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,9,0 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65907-71:
(7*6)+(6*5)+(5*9)+(4*0)+(3*7)+(2*7)+(1*1)=153
153 % 10 = 3
So 65907-71-3 is a valid CAS Registry Number.

65907-71-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-nitro-4,5-dimethoxystyrene

1.2 Other means of identification

Product number -
Other names 4,5-dimethoxy-2-nitrostyrene

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:65907-71-3 SDS

65907-71-3Relevant articles and documents

Direct Arylation of Distal and Proximal C(sp3)-H Bonds of t-Amines with Aryl Diazonium Tetrafluoroborates via Photoredox Catalysis

Mondal, Pradip Kumar,Tiwari, Sandip Kumar,Singh, Pushpendra,Pandey, Ganesh

, p. 17184 - 17196 (2021/12/02)

A visible light-mediated arylation protocol for t-amines has been reported through the coupling of γ- and α-amino alkyl radicals with different aryl diazonium salts using Ru(bpy)3Cl2·6H2O as a photocatalyst. Structurally different 9-aryl-9,10-dihydroacridine, 1-aryl tetrahydroisoquinoline, hexahydropyrrolo[2,1-a]isoquinoline, and hexahydro-2H-pyrido[2,1-a]isoquinoline frameworks with different substitution patterns have been synthesized in good yield using this methodology.

Native Chemical Ligation Directed by Photocleavable Peptide Nucleic Acid (PNA) Templates

Middel, Stephen,Panse, Cornelia H.,Nawratil, Swantje,Diederichsen, Ulf

, p. 2328 - 2332 (2017/11/10)

A novel peptide–peptide ligation strategy is introduced that has the potential to provide peptide libraries of linearly or branched coupled fragments and will be suited to introduce simultaneous protein modifications at different ligation sites. Ligation

An o-nitrobenzyl scaffold for peptide ligation: Synthesis and applications

Marinzi, Chiara,Offer, John,Longhi, Renato,Dawson, Philip E.

, p. 2749 - 2757 (2007/10/03)

Chemical ligation approaches facilitate the chemoselective assembly of unprotected peptides in aqueous solution. Here, two photolabile auxiliaries are described that enlarge the applicability of native chemical ligation to non-cysteine targets. The auxili

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