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1H-Indazole,1-(1-methylethyl)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83482-91-1

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83482-91-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83482-91-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,4,8 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 83482-91:
(7*8)+(6*3)+(5*4)+(4*8)+(3*2)+(2*9)+(1*1)=151
151 % 10 = 1
So 83482-91-1 is a valid CAS Registry Number.

83482-91-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-isopropylindazole

1.2 Other means of identification

Product number -
Other names 1-isopropyl-1H-indazole

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:83482-91-1 SDS

83482-91-1Relevant academic research and scientific papers

HURAT1 (human urate anion transporter 1) inhibitors and application thereof

-

Paragraph 0064; 0086; 0086; 0088, (2018/11/22)

The invention belongs to the field of medicinal chemistry and particularly relates to hURAT1 (human urate anion transporter 1) inhibitors and an application thereof. Specifically, the hURAT1 inhibitors are compounds with structure shown as formula (I) or (II) in the description or pharmaceutically acceptable salts of the compounds. Experiments prove that the compounds have good inhibition effect on uric acid transport of the hURAT1 in an HEK293 transfection cell, which shows that the compounds have good application prospect in treatment of hyperuricemia or gout.

CLEAVAGE OF THE N-N BOND IN 1-SUBSTITUTED INDAZOLES UNDER THE INFLUENCE OF ARYLLITHIUM COMPOUNDS

Tertov, B. A.,Onishchenko, P. P.,Koshchienko, Yu. V.,Suvorova, G. M.,Malysheva, E. N.

, p. 823 - 826 (2007/10/02)

Upon reaction with aryllithium compounds (phenyllithium and m-tolyllithium) m-methyl- and 1-isopropylindazoles undergo cleavage at the N-N bond to give N-substituted 2-aminobenzophenones.The heterocyclic ring of 1-isopropyl-3-phenylindazole also undergoes cleavage at this bond under the influence of phenyllithium.

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