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151585-93-2

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151585-93-2 Usage

General Description

2-Amino-6-fluorobenzaldehyde is a chemical compound with the molecular formula C7H6FNO. It is a pale yellow solid with a strong, pungent odor. 2-Amino-6-fluorobenzaldehyde is commonly used as an intermediate in the pharmaceutical industry for the synthesis of various drugs, particularly those used in the treatment of central nervous system disorders. Additionally, 2-Amino-6-fluorobenzaldehyde is also used as a reagent in organic synthesis, particularly in the preparation of Schiff bases and other organic compounds. It is important to handle this chemical with caution, as it is toxic if ingested or inhaled, and may cause irritation to the skin and eyes.

Check Digit Verification of cas no

The CAS Registry Mumber 151585-93-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,5,8 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 151585-93:
(8*1)+(7*5)+(6*1)+(5*5)+(4*8)+(3*5)+(2*9)+(1*3)=142
142 % 10 = 2
So 151585-93-2 is a valid CAS Registry Number.

151585-93-2SDS

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 2-Amino-6-fluorobenzaldehyde

1.2 Other means of identification

Product number -
Other names 2-Furanmethanol,5-(2-amino-6-fluoro-9H-purin-9-yl)tetrahydro-,(2S,5R)

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:151585-93-2 SDS

151585-93-2Relevant articles and documents

Heavy-Atom Tunneling Through Crossing Potential Energy Surfaces: Cyclization of a Triplet 2-Formylarylnitrene to a Singlet 2,1-Benzisoxazole

Fausto, Rui,McMahon, Robert J.,Nunes, Cláudio M.,Roque, José P. L.,Viegas, Luís P.,Wood, Samuel A.

, p. 17622 - 17627 (2020)

Not long ago, the occurrence of quantum mechanical tunneling (QMT) chemistry involving atoms heavier than hydrogen was considered unreasonable. Contributing to the shift of this paradigm, we present here the discovery of a new and distinct heavy-atom QMT

HETEROCYCLIC COMPOUNDS AND THEIR USE AS INHIBITORS OF PI3K ACTIVITY

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Page/Page column 100, (2012/01/15)

Substituted bicyclic heteroaryls and compositions containing them, for the treatment of general inflammation, arthritis, rheumatic diseases, osteoarthritis, inflammatory bowel disorders, inflammatory eye disorders, inflammatory or unstable bladder disorde

GONADOTROPIN-RELEASING HORMONE RECEPTOR ANTAGONISTS AND METHODS RELATING THERETO

-

, (2008/12/04)

GnRH receptor antagonists are disclosed which have utility in the treatment of a variety of sex-hormone related conditions in both men and women. The compounds of this invention have the structure, wherein R1a, R1b, R1c, R1d, R2, R2a, and A are as defined herein, including stereoisomers, esters, solvates and pharmaceutically acceptable salts thereof. Also disclosed are compositions containing a compound of this invention in combination with a pharmaceutically acceptable carrier, as well as methods relating to the use thereof for antagonizing gonadotropin-releasing hormone in a subject in need thereof.

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