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(5-aMino-2-nitro-phenyl)-Methanol is an organic compound that serves as a key reactant in the synthesis of various antimicrobial agents.

77376-03-5

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77376-03-5 Usage

Uses

Used in Pharmaceutical Industry:
(5-aMino-2-nitro-phenyl)-Methanol is used as a reactant for the preparation of antimicrobial biscationic 2-(phenoxyphenyl)indoles and 1-benzofurans, which are compounds with potential applications in the development of new antibiotics and antimicrobial drugs. These agents can help combat drug-resistant bacteria and contribute to the treatment and prevention of various infections.

Check Digit Verification of cas no

The CAS Registry Mumber 77376-03-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,3,7 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 77376-03:
(7*7)+(6*7)+(5*3)+(4*7)+(3*6)+(2*0)+(1*3)=155
155 % 10 = 5
So 77376-03-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2O3/c8-6-1-2-7(9(11)12)5(3-6)4-10/h1-3,10H,4,8H2

77376-03-5SDS

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 (5-Amino-2-nitrophenyl)methanol

1.2 Other means of identification

Product number -
Other names 5-Amino-2-nitro-benzylalkohol

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:77376-03-5 SDS

77376-03-5Relevant academic research and scientific papers

Substituted 2-nitrobenzyltrichloroacetate esters for photodirected oligonucleotide detritylation in solid films

Serafinowski, Pawel J.,Garland, Peter B.

supporting information; experimental part, p. 3284 - 3291 (2009/02/05)

Oligonucleotide microarray fabrication by chemical synthesis using photoacid generators in solid films could have advantages over existing methods, but has not matched the accuracy of conventional synthesis where detritylation is performed with acid solut

O-nitrobenzyl photolabile protecting groups with red-shifted absorption: Syntheses and uncaging cross-sections for one- And two-photon excitation

Aujard, Isabelle,Benbrahim, Chouaha,Gouget, Marine,Ruel, Odile,Baudin, Jean-Bernard,Neveu, Pierre,Jullien, Ludovic

, p. 6865 - 6879 (2007/10/03)

We evaluated the o-nitrobenzyl platform for designing photolabile protecting groups with red-shifted absorption that could be photolyzed upon one- and two-photon excitation. Several synthetic pathways to build different conjugated o-nitrobenzyl backbones,

PROPIONAMIDE DERIVATIVES USEFUL AS ANDROGEN RECEPTOR MODULATORS

-

Page 40, (2010/02/10)

Compounds of formula (I) wherein R1 to R4, X and A are as defined in the claims and pharmaceutically acceptable salts and esters thereof, are disclosed. The compounds of formula (I) possess utility as tissue-selective androgen receptor modulators (SARM) and are useful in hormonal therapy, e.g. in the treatment or prevention of male hypogonadism and age-related conditions such as andropause.

γ-L-glutamyl-4-nitroanilide derivatives and process for determining γ-GTP activity using the same

-

, (2008/06/13)

A γ-L-glutamyl-4-nitroanilide derivative of the formula: STR1 wherein R is a lower hydroxyalkyl group, is suitable as a substrate for determining γ-GTP activity.

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