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2-Pyrimidinecarboxaldehyde, oxime (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83959-46-0

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83959-46-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83959-46-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,9,5 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 83959-46:
(7*8)+(6*3)+(5*9)+(4*5)+(3*9)+(2*4)+(1*6)=180
180 % 10 = 0
So 83959-46-0 is a valid CAS Registry Number.

83959-46-0SDS

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 pyrimidine-2-carbaldehyde oxime

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:83959-46-0 SDS

83959-46-0Upstream product

83959-46-0Downstream Products

83959-46-0Relevant academic research and scientific papers

Development of an efficient, scalable route for the preparation of a novel insulin-like growth factor-1 receptor modulator

Kumar, C.H. Vinod,Kavitake, Santosh,Kumar, Sythana Suresh,Cornwall, Philip,Ashok, Mithun,Bhagat, Sagar,Manjunatha, Sulur G.,Nambiar, Sudhir

, p. 1416 - 1421 (2012)

A chromatography-free and efficient synthesis of insulin-like growth factor-1 receptor (IGF-1R) modulator is reported. Herein we describe an improved synthesis for the target compound, which features facile introduction of a novel pyrrolidinyl-pyrimidyl isoxazole 8, via in situ sulfone displacement by fluorine. The overall process consists of six chemical steps and five isolations, with introduction of the expensive triheterocyclic unit 8 towards the end of the synthesis.

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