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212268-13-8

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212268-13-8 Usage

General Description

6-FLUORO-3,4-PYRIDINEDIAMINE is a chemical compound with the molecular formula C5H6FN3. It is a derivative of pyridine and is primarily used as an intermediate in the production of pharmaceuticals, agrochemicals, and other organic compounds. 6-FLUORO-3,4-PYRIDINEDIAMINE is a white solid with a density of 1.36 g/cm3 and a melting point of 179-181°C. It is a key building block in the synthesis of various biologically active molecules and is used in the pharmaceutical industry for the development of new drugs. Additionally, 6-FLUORO-3,4-PYRIDINEDIAMINE is also used in the production of dyes, pigments, and other specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 212268-13-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,2,2,6 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 212268-13:
(8*2)+(7*1)+(6*2)+(5*2)+(4*6)+(3*8)+(2*1)+(1*3)=98
98 % 10 = 8
So 212268-13-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H6FN3/c6-3-1-4(7)5(8)9-2-3/h1-2H,7H2,(H2,8,9)

212268-13-8SDS

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 5-fluoropyridine-2,3-diamine

1.2 Other means of identification

Product number -
Other names 5-fluoropyridine-2.3-diamine

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:212268-13-8 SDS

212268-13-8Relevant articles and documents

Benzimidazole derivatives, their preparation and their application in medicine and pharmacology (by machine translation)

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Paragraph 0381-0382, (2019/07/16)

The invention relates to a new control or inhibit indocyanine 2, 3 - dioxygenase (IDO) activity of the benzimidazole derivatives, their preparation and their application in medicine and pharmacology. Specifically, the invention relates to a compound of general formula (I) compound of formula and its pharmaceutically acceptable salt, containing the compound or its pharmaceutically acceptable salt of the pharmaceutical composition, the use of the compound or its pharmaceutically acceptable salts for treating and/or preventing the relevance of the IDO-mediated disease, especially a tumor of the method and the compound or its pharmaceutically acceptable salts thereof. The invention also relates to the compound or its pharmaceutically acceptable salt or containing the compound or its pharmaceutically acceptable salts for the preparation of a pharmaceutical composition for treating and/or preventing the relevance of the IDO-mediated disease, in particular of the use of the drug in the tumor. Wherein the general formula (I) of each substituent is as defined in the specification. (by machine translation)

HETERO RING-FUSED IMIDAZOLE DERIVATIVE HAVING AMPK ACTIVATING EFFECT

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, (2013/07/25)

Disclosed is a compound which is useful as an AMPK activator. A compound represented by the formula: its pharmaceutically acceptable salt, or a solvate thereof, wherein a group represented by the formula: is a group represented by the formula: R1 /s

CGRP RECEPTOR ANTAGONISTS

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Page/Page column 66, (2010/11/08)

Compounds of Formula (I): and Formula (II): (where variables R2, R4, A, B, D, W, X, Y and Z are as defined herein) useful as antagonists of CGRP receptors and useful in the treatment or prevention of diseases in which the CGRP is involved, such as headache, migraine and cluster headache. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which CGRP is involved.

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