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3-amino-5-chloropicolinonitrile is a chemical compound with the molecular formula C6H4ClN3. It is a derivative of picolinonitrile, characterized by the presence of a chloro group at the 5th position and an amino group at the 3rd position. 3-amino-5-chloropicolinonitrile is known for its reactivity and versatility, making it a valuable building block in the synthesis of various organic compounds and pharmaceuticals.

408538-29-4

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408538-29-4 Usage

Uses

Used in Pharmaceutical Industry:
3-amino-5-chloropicolinonitrile is used as a key intermediate in the synthesis of heterocyclic and bioactive molecules for pharmaceutical applications. Its unique structure and reactivity contribute to the development of new drugs with potential therapeutic benefits.
Used in Chemical Industry:
In the chemical industry, 3-amino-5-chloropicolinonitrile serves as an important building block for the production of various organic compounds. Its properties and structure enable the creation of new materials and compounds with diverse applications in different sectors.
Overall, 3-amino-5-chloropicolinonitrile is a versatile and valuable compound in both the pharmaceutical and chemical industries, playing a crucial role in the synthesis and development of innovative products.

Check Digit Verification of cas no

The CAS Registry Mumber 408538-29-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,8,5,3 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 408538-29:
(8*4)+(7*0)+(6*8)+(5*5)+(4*3)+(3*8)+(2*2)+(1*9)=154
154 % 10 = 4
So 408538-29-4 is a valid CAS Registry Number.

408538-29-4SDS

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-amino-5-chloropyridine-2-carbonitrile

1.2 Other means of identification

Product number -
Other names 3-amino-5-chloro-pyridine-2-carbonitrile

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:408538-29-4 SDS

408538-29-4Relevant articles and documents

IDENTIFICATION AND USE OF ERK5 INHIBITORS

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Page/Page column 121, (2019/10/01)

The present invention covers heterocyclic compounds of general formula (I) in which T, U, Y, Z, R1 and R3 are as defined herein, methods of preparing said compounds, intermediate compounds useful for preparing said compounds, pharmaceutical compositions and combinations comprising said compounds and the use of said compounds for manufacturing pharmaceutical compositions for the treatment or prophylaxis of diseases, in particular of cancer disorders, as a sole agent or in combination with other active ingredients.

FUSED HETEROARYL PYRIDYL AND PHENYL BENZENESUFLONAMIDES AS CCR2 MODULATORS FOR THE TREAMENT OF INFLAMMATION

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Page/Page column 55, (2009/03/07)

Compounds are provided that act as potent antagonists of the CCR2 receptor. The compounds are generally aryl sulfonamide derivatives and are useful in pharmaceutical compositions, methods for the treatment of CCR2- mediated diseases and as controls in assays for the identification of CCR2 antagonists. A compound of the formula (I) or a salt thereof: where: R1 and R2 are each independently hydrogen, halogen, C1-8alkyl, -CN. or C1-8 haloalkyl, provided that at least one of R11or R2 is other than hydrogen; each R3 is independently hydrogen; R4 is hydrogen; R5 is halogen or C1-8 alkyl; R6 is hydrogen; X1 is CR7, N or NO; X2 and X4 are N or NO; X3 is CR7; X6 and X7 are each independently selected from CR7, N, and NO; each R7 is independently selected from the group consisting of hydrogen, halogen, substituted or unsubstituted C2-8 alkyl, substituted or unsubstituted C2-8 alkeπyl, substituted or unsubstituted C2-8 alkynyl, -CN. =O, -NO2, -OR6, -OC(O)R8, -CO2R8, -C(O)R8, -C(O)NR0R8, -OC(O)NR9R8, -NR10C(O)R8, -NR10C(O)NR9R8, -NR9R8, -NR10CO2R8, -SR8, -S(O)R8, -S(O)2R8, -S(O)2NR9R8, -NR10S(O)2R8, substituted or unsubstituted C6-10 aryl, substituted or unsubstituted 5- to 10-membered heteroaryl and substituted or unsubstituted 3- to 10-membered heterocyclyl;

HETEROARYL SULFONAMIDES AND CCR2

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Page/Page column 174, (2008/06/13)

Compounds are provided that act as potent antagonists of the CCR2 receptor. Animal testing demonstrates that these compounds are useful for treating inflammation, a hallmark disease for CCR2. The compounds are generally aryl sulfonamide derivatives and are useful in pharmaceutical compositions, methods for the treatment of CCR2-mediated diseases, and as controls in assays for the identification of CCR2 antagonists.

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