6-Chloro-1H-pyrazolo[4,3-c]pyridine CAS 1206979-33-0

• Iden­ti­fi­ca­tion
• Prop­er­ties
• Safe­ty Data
• Spec­i­fi­ca­tions & Oth­er Information
• Links
• Quick Inquiry

Iden­ti­fi­ca­tion

CAS Number

1206979-33-0

Name

6-Chloro-1H-pyrazolo[4,3-c]pyridine

Syn­onyms

1206979-33-0[RN]
1H-Pyrazolo[4,3-c]pyridine, 6-chloro-
[ACD/​Index Name]
6-Chlor-1H-pyrazolo[4,3-c]pyridin
[Ger­man]
[ACD/IUPAC Name]
6-chloro-1H-pyrazolo[4,3-c]pyridine
[ACD/IUPAC Name]
6-Chloro-1H-pyrazolo[4,3-c]pyridine
[French]
[ACD/IUPAC Name]
MFCD17010105
[MDL num­ber]
Unver­i­fied
2-(Amino(phenyl)methylene)malononitrile
20300-02-1
[RN]
4-Chloro-1H-pyrazolo[4,3-c]pyridine
[ACD/IUPAC Name]
4649-09-6
[RN]
6-chloro-1h-pyrazolo4,3-cpyridine
6-chloro-1h-pyrazolo[4,3-c]pyridine(wxc01805)
6-Chloro-1H-pyrazolo[4,3-c]pyridine,
6-chloro-2H-pyrazolo[4,3-c]pyridine
6-Chloro-5-azain­­da­­zole
871836-51-0
[RN]
95%
AGN-PC-0BMJND
CTK8B5457
Mol­­Port-023-219-348
PS-J-068
Thio­phene-2-thio­­car­box­am­ide

SMILES

Clc1cc2[nH]ncc2cn1

Std­InChI

InChI=1S/C6H4ClN3/c7-6-1-5-4(2-8-6)3-9-10-5/h1-3H,(H,9,10)

Std­InChIKey

AAJIQI­W­PVI­W­C­­GA-UHF­F­­FAOYSA-N

Mol­e­c­u­lar Formula

C6H4ClN3

Mol­e­c­u­lar Weight

153.569

MDL Number

MFCD17010105

Prop­er­ties

Appear­ance

Light yel­low to brown solid

Sol­u­bil­i­ty

Sol­u­ble in ethanol

Safe­ty Data

RIDADR 

NONH for all modes of transport

WGK Germany

3

Spec­i­fi­ca­tions and Oth­er Infor­ma­tion of Our 6-Chloro-1H-pyrazolo[4,3-c]pyridine CAS 1206979-33-0

Iden­ti­fi­ca­tion Methods

HNMR, HPLC

Puri­ty

98% min

Shelf Life

2 years

Stor­age

Under room tem­per­a­ture away from light

Known Appli­ca­tion

1. Phar­ma­ceu­ti­cal inter­me­di­ates : This is its most com­mon use. This type of struc­ture is wide­ly used to syn­the­size tar­get­ed kinase drugs (such as PI3K, JAK, BTK inhibitors) or cen­tral ner­vous sys­tem drugs. For exam­ple, it is used as a core skele­ton in the syn­the­sis route of anti-can­cer, anti-inflam­­ma­­to­ry, antivi­ral and neu­ro­log­i­cal dis­ease drugs.
2. Drug lead com­pound design : Pyra­zolopy­ri­dine struc­ture is val­ued in med­i­c­i­nal chem­istry for its bio­log­i­cal activ­i­ty. The chlo­rine atom site of this com­pound can be used for fur­ther func­tion­al group intro­duc­tion reac­tions (such as Suzu­ki or Buch­wald cou­pling reac­tions) to con­struct com­plex molecules.
3. Sci­en­tif­ic research use : Com­mon­ly used in high-through­put screen­ing (HTS) or struc­­ture-activ­i­­ty rela­tion­ship stud­ies (SAR) in the new drug devel­op­ment stage.

Gen­er­al View of Documents

Links

This prod­uct is devel­oped by our R&D com­pa­ny Cam­ing Phar­ma­ceu­ti­cal Ltd (https://​www​.cam​ing​.com/).

Quick Inquiry

Fill out our inquiry form and one of our experts will be in touch with you shortly.