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2-Butyl-2H-pyrazol-3-ylamine is an organic compound with the chemical formula C8H14N2. It is a derivative of pyrazole, a heterocyclic compound consisting of a five-membered aromatic ring with two nitrogen atoms. The 2-butyl group attached to the pyrazole ring gives 2-BUTYL-2H-PYRAZOL-3-YLAMINE its unique structure and properties. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its potential applications in the development of new drugs and chemicals, research on 2-butyl-2H-pyrazol-3-ylamine and its derivatives is of interest to the scientific community.

3524-17-2

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3524-17-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3524-17-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,2 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3524-17:
(6*3)+(5*5)+(4*2)+(3*4)+(2*1)+(1*7)=72
72 % 10 = 2
So 3524-17-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H13N3/c1-2-3-6-10-7(8)4-5-9-10/h4-5H,2-3,6,8H2,1H3

3524-17-2SDS

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 2-butylpyrazol-3-amine

1.2 Other means of identification

Product number -
Other names 1-Butyl-5-amino-pyrazol

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:3524-17-2 SDS

3524-17-2Upstream product

3524-17-2Downstream Products

3524-17-2Relevant academic research and scientific papers

Stable Yellow Imidazolium Compounds

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Paragraph 0240; 0241, (2018/04/13)

Described herein is a yellow imidazolium chromophore having a structure according to Formula V.

Process for preparing pyrazolopyridine compounds

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, (2008/06/13)

Compounds of the formula (I): STR1 wherein R4 is hydrogen, D is oxygen or NR6, R1, R3, R6, R7 and R8 have defined values, and n is 1 or 2 are produced by internally cyclizing a compound of the formula (XV): STR2 wherein R19 is a value of R1 or hydrogen and, if R19 is hydrogen, reacting the cyclization product with R1 --Br and a weak base such as potassium carbonate.

CNS-Depressant pyrazolopyridines

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, (2008/06/13)

Compounds of the formula (I): STR1 wherein R1, R3, R4, R7 and R8 are as described herein, D is oxygen or NR6, n is 1 or 2 and the physiologically acceptable salts thereof useful in reducing anxiety in an animal such as man. The compounds are potent anxiolytics having reduced side effects compared to known anxiolytics. Also pharmaceutical compositions, intermediates and methods of treatment and synthesis are described.

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