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90178-82-8

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90178-82-8 Usage

Uses

Different sources of media describe the Uses of 90178-82-8 differently. You can refer to the following data:
1. 3-Formyl-4-nitrobenzonitrile is the tri-substitiuted derivative of benzene. 3-Formyl-4-nitrobenzonitrile is an intermediate used in the synthetic preparation of various pharmaceuticals exhibiting larg e spectrum of activity.
2. 3-Formyl-4-nitrobenzonitrile is the tri-substitiuted derivative of benzene. 3-Formyl-4-nitrobenzonitrile is an intermediate used in the synthetic preparation of various pharmaceuticals exhibiting large spectrum of activity.

Check Digit Verification of cas no

The CAS Registry Mumber 90178-82-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,1,7 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 90178-82:
(7*9)+(6*0)+(5*1)+(4*7)+(3*8)+(2*8)+(1*2)=138
138 % 10 = 8
So 90178-82-8 is a valid CAS Registry Number.

90178-82-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Formyl-4-nitrobenzonitrile

1.2 Other means of identification

Product number -
Other names Benzonitrile,3-formyl-4-nitro

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:90178-82-8 SDS

90178-82-8Relevant articles and documents

Development of a Practical Synthesis of a Farnesyltransferase Inhibitor

Shi, Zhongping,Fan, Junying,Kronenthal, David R.,Mudryk, Boguslaw M.

, p. 1534 - 1540 (2018/11/23)

The development of a new and practical synthesis for a farnesyltransferase inhibitor 1 is described. The new route started from 2-nitro-5-cyanotoluene (9) and afforded desired 1 in eight chemical transformations. The key step involved formation of sulfonamide 13 from a hindered β-hydroxyamine 12 through an in situ protection of the hydroxyl group by forming TMS ether. Ultimately, this new route was successfully demonstrated to generate >10 kg of API in 29% overall yield.

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