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98027-52-2

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98027-52-2 Usage

General Description

1-Acetyl-4-iodo-1H-pyrazole is a chemical compound with the molecular formula C5H5IN2O. It is a pyrazole derivative that is typically used in pharmaceutical research and development. The compound is characterized by the presence of an acetyl group and an iodine atom attached to a pyrazole ring. It has potential applications in the synthesis of biologically active molecules and pharmaceutical drugs. The compound may also have other industrial or research uses, such as in the development of new materials or in chemical synthesis processes. Overall, 1-Acetyl-4-iodo-1H-pyrazole is a versatile chemical compound with potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 98027-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,0,2 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 98027-52:
(7*9)+(6*8)+(5*0)+(4*2)+(3*7)+(2*5)+(1*2)=152
152 % 10 = 2
So 98027-52-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H5IN2O/c1-4(9)8-3-5(6)2-7-8/h2-3H,1H3

98027-52-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-iodopyrazol-1-yl)ethanone

1.2 Other means of identification

Product number -
Other names 4-iodo-1-acetylpyrazole

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:98027-52-2 SDS

98027-52-2Relevant articles and documents

Histone Deacetylase Inhibitors

-

Paragraph 0479, (2013/12/04)

This invention relates to generally inhibiting histone deacetylase (“HDAC”) enzymes (e.g., HDAC1, HDAC2, and HDAC3).

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