(4-iodo-1H-pyrazol-1-yl)acetic acid

Base Information

Chemical Name:(4-iodo-1H-pyrazol-1-yl)acetic acid
CAS No.:6752-13-2
Molecular Formula:C₅H₅IN₂O₂
Molecular Weight:252.011
Hs Code.:2933199090
European Community (EC) Number:847-079-5
Mol file:6752-13-2.mol

Synonyms:(4-iodo-1H-pyrazol-1-yl)acetic acid;6752-13-2;2-(4-iodo-1H-pyrazol-1-yl)acetic acid;2-(4-iodopyrazol-1-yl)acetic acid;MFCD08558964;2-(4-iodo-pyrazol-1-yl)acetic acid;SCHEMBL15485301;VYRSJDHAOMNMLF-UHFFFAOYSA-N;2-(4-Iodo-1-pyrazolyl)acetic Acid;BBL036698;STL559077;AKOS005174082;2-(4-iodo-1H-pyrazol-1-yl)aceticacid;SY344694;VS-13635;DB-121688;CS-0231413;EN300-1082655;AO-022/43514250;F8886-7537;Z1227758254

Suppliers and Price of (4-iodo-1H-pyrazol-1-yl)acetic acid

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Crysdot
2-(4-Iodo-1H-pyrazol-1-yl)aceticacid 97%
5g
$ 752.00

CHESS?
KX001503:(4-iodo-1H-pyrazol-1-yl)aceticacid 97
5 g
$ 1020.00

Apolloscientific
2-(4-Iodopyrazol-1-yl)aceticacid
250mg
$ 73.00

Apolloscientific
2-(4-Iodopyrazol-1-yl)aceticacid
5g
$ 607.00

Apolloscientific
2-(4-Iodopyrazol-1-yl)aceticacid
1g
$ 209.00

AK Scientific
(4-Iodo-1H-pyrazol-1-yl)aceticacid
250mg
$ 187.00

Total 6 raw suppliers

Chemical Property of (4-iodo-1H-pyrazol-1-yl)acetic acid

Chemical Property:

XLogP3:0.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:251.93957
Heavy Atom Count:10
Complexity:142

Purity/Quality:

98%min ^*data from raw suppliers

2-(4-Iodo-1H-pyrazol-1-yl)aceticacid 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=C(C=NN1CC(=O)O)I

Technology Process of (4-iodo-1H-pyrazol-1-yl)acetic acid

There total 2 articles about (4-iodo-1H-pyrazol-1-yl)acetic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 82.0%

: 3469-69-0
4-iodopyrazole

: 5292-43-3
bromoacetic acid tert-butyl ester

: 6752-13-2
2-(4-iodo-1H-pyrazol-1-yl)acetic acid

Guidance literature:: 4-iodopyrazole; bromoacetic acid tert-butyl ester; With caesium carbonate; In acetonitrile; at 80 ℃; for 12h;

With trifluoroacetic acid; In acetonitrile; at 20 ℃; for 1h;

Reference yield:

: 6752-13-2
2-(4-iodo-1H-pyrazol-1-yl)acetic acid

Guidance literature:: 4-Iod-pyrazol, 2-Ethoxyethanol (od. Toluol), Brom-essigsaeureethylester, K2CO3 (100grad);

Reference yield: 73.0%

: (S)-4-(4-chlorophenyl)-2-ethynyl-3,6,9-trimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine

: 6752-13-2
2-(4-iodo-1H-pyrazol-1-yl)acetic acid

: (S)-2-(4-((4-(4-chlorophenyl)-3,6,9-trimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-2-yl)ethynyl)-1H-pyrazol-1-yl)acetic acid

Guidance literature:: With copper(l) iodide; trans-bis(triphenylphosphine)palladium dichloride; triethylamine; In N,N-dimethyl-formamide; at 80 ℃; for 1h; Inert atmosphere;