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86810-74-4

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86810-74-4 Usage

Molecular weight

235.33 g/mol

Physical state

Yellow crystalline solid

Uses

a. Intermediate in the production of pharmaceuticals
b. Intermediate in the production of agrochemicals
c. Used in the synthesis of other organic compounds
d. Reagent in chemical reactions and synthesis processes

Chemical structure features

a. Nitro group (-NO2) attached to a benzene ring
b. Sulfanyl group (-S) attached to a 2,2-dimethylpropyl group
c. 2,2-Dimethylpropyl group attached to the benzene ring

Chemical reactivity

a. Ability to participate in various types of chemical reactions due to the presence of a nitro group and a sulfanyl group
b. Versatile compound in organic chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 86810-74-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,8,1 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86810-74:
(7*8)+(6*6)+(5*8)+(4*1)+(3*0)+(2*7)+(1*4)=154
154 % 10 = 4
So 86810-74-4 is a valid CAS Registry Number.

86810-74-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,2-dimethylpropylsulfanyl)-4-nitrobenzene

1.2 Other means of identification

Product number -
Other names -

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:86810-74-4 SDS

86810-74-4Relevant articles and documents

USP30 INHIBITORS AND USES THEREOF

-

Paragraph 00305-00306, (2021/03/19)

The present invention provides compounds, compositions thereof, and methods of using the same for the inhibition of USP30, and the treatment of USP30-mediated disorders.

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