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113140-14-0

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113140-14-0 Usage

Description

7-chloro-5-Methyl-1H-pyrazolo[4,3-b]pyridin-3-aMine is a pyrazolo[4,3-b]pyridine derivative characterized by the molecular formula C8H7ClN4. This chemical compound features a chlorine atom and a methyl group attached to the pyrazole ring, contributing to its unique structure and properties. Its potential applications in medicinal chemistry make it a promising candidate for the development of pharmaceutical drugs that target specific biological pathways or receptors.

Uses

Used in Pharmaceutical Drug Development:
7-chloro-5-Methyl-1H-pyrazolo[4,3-b]pyridin-3-aMine is used as a key intermediate in the synthesis of new chemical entities for the development of pharmaceutical drugs. Its unique structure allows for the design of compounds with potential pharmacological activity, targeting specific biological pathways or receptors.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 7-chloro-5-Methyl-1H-pyrazolo[4,3-b]pyridin-3-aMine serves as a valuable research tool for understanding the structure-activity relationships of pyrazolo[4,3-b]pyridine derivatives. This knowledge can be applied to optimize the properties and efficacy of newly synthesized compounds.
Used in Drug Discovery:
7-chloro-5-Methyl-1H-pyrazolo[4,3-b]pyridin-3-aMine is utilized in drug discovery processes to identify novel therapeutic agents with potential applications in various diseases and conditions. Its unique chemical properties make it a versatile building block for the development of innovative drugs.
However, it is important to note that further research and investigation are required to fully understand and harness the potential of 7-chloro-5-Methyl-1H-pyrazolo[4,3-b]pyridin-3-aMine in these applications.

Check Digit Verification of cas no

The CAS Registry Mumber 113140-14-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,1,4 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 113140-14:
(8*1)+(7*1)+(6*3)+(5*1)+(4*4)+(3*0)+(2*1)+(1*4)=60
60 % 10 = 0
So 113140-14-0 is a valid CAS Registry Number.

113140-14-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-Chloro-5-methyl-1H-pyrazolo[4,3-b]pyridin-3-amine

1.2 Other means of identification

Product number -
Other names 3-amino-7-chloro-5-methyl-1H-pyrazolo[4,3-b]pyridine

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:113140-14-0 SDS

113140-14-0Downstream Products

113140-14-0Relevant articles and documents

Pharmaceutically useful pyrazolo[4,3-b]pyridines

-

, (2008/06/13)

A compound of the formula (I) or a salt or solvate thereof: STR1 in which: R0 is hydrogen or C1-6 alkyl; or together with R3 is C4-6 polymethylene; R1 and R2 are both hydrogen; or R1 is hydrogen, C1-6 alkyl; and R2 is CN; CR5 R6 Y where R5 and R6 are independently selected from hydrogen and C1-4 alkyl and Y is selected from hydrogen, OR7 or SR7 where R7 is hydrogen, C1-4 alkyl or C2-4 alkanoyl, and NR8 R9 where R8 and R9 are independently hydrogen, C1-4 alkyl, C2-4 alkenyl or C2-4 alkanoyl or together are C4-6 polymethylene; or COR10 where R10 is OH or C1-4 alkyl, or COR10 is a pharmaceutically acceptable ester or amide, or R2 is hydrogen, C1-6 alkyl, or phenyl optionally substituted by halogen, CF3, C1-4 alkoxy or C1-4 alkyl, and R1 is CN, CR5 R6 Y or COR10 as defined for R2 above; or R1 and R2 together form C3 -C6 polymethylene optionally substituted by C1 -C4 alkyl; R3 is hydrogen; or C1-10 alkyl or C3-10 cycloalkyl, either optionally substituted by hydroxy, C1-4 alkoxy, thiol, C1-4 alkylthio or NR11 R12 wherein R11 and R12 are independently hydrogen, C1-6 alkyl or C2-7 alkanoyl or together are C3-6 polymethylene; C2-10 alkenyl; or phenyl optionally substituted by one or two of halogen, CF3, C1-4 alkoxy, C1-4 alkyl, hydroxy, nitro, cyano, C2-10 acyloxy, NR13 R14 wherein R13 and R14 are independently selected from hydrogen, C1-6 alkyl, or C2-7 alkanoyl; or COR15 wherein R15 is hydroxy, C1-6 alkoxy or NR16 R17 wherein R16 and R17 are independently selected from hydrogen or C1-6 alkyl; or R3 is a mono- or fused bi-cyclic heteroaryl group having up to ten atoms in the aromatic ring(s), not more than two of which are selected from nitrogen, oxygen or sulphur, other than those containing basic nitrogen, optionally substituted by one or two substituents selected from halogen, CF3, C1-4 alkoxy, C1-4 alkyl, hydroxy, nitro, cyano, C2-10 acyloxy, NR23 R24 wherein R23 and R24 are independently selected from hydrogen, C1-6 alkyl, C2-7 alkanoyl or C1-6 alkylsulphonyl; or COR25 wherein R25 is hydroxy, C1-6 alkoxy or NR26 R27 wherein R26 and R27 are independently selected from hydrogen or C1-6 alkyl; R4 is hydrogen, or C1-4 alkyl, phenyl or benzyl, each of which is optionally substituted in the phenyl ring by one or two of halogen, CF3, C1-4 alkoxy or C1-4 alkyl and is attached at nitrogen atom 1 or 2; and Rx is C1-6 alkyl, halogen, nitro, NR18 R19 where R18 and R19 are independently hydrogen, C1-6 alkyl or C2-7 alkanoyl, nitrile, COOH, CONH2 ; phenyl or benzyl optionally substituted by one or two of halogen, nitro, C1-6 alkoxy, hydroxy, C2-7 alkanoyloxy, NR18 R19, C1-6 alkyl, CF3, CN; thienyl, furyl or pyrryl optinoally N-substituted by C1-6 alkyl, with the proviso that R0 and R3 are not both hydrogen when R1 is hydrogen and R2 and Rx are methyl, is useful for treating inflammatory or allergic conditions.

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