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1-methyl-3-pyridin-3-ylurea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39805-01-1

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39805-01-1 Usage

Physical Appearance

White crystalline solid

Molecular Weight

150.18 g/mol

Chemical Classification

Urea derivative

Structural Features

Pyridine ring and a methyl substituent

Usage

Intermediate in the synthesis of various pharmaceutical compounds

Potential Applications

Herbicide

Industries of Interest

Pharmaceutical and agrochemical sectors

Check Digit Verification of cas no

The CAS Registry Mumber 39805-01-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,8,0 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 39805-01:
(7*3)+(6*9)+(5*8)+(4*0)+(3*5)+(2*0)+(1*1)=131
131 % 10 = 1
So 39805-01-1 is a valid CAS Registry Number.

39805-01-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-3-pyridin-3-ylurea

1.2 Other means of identification

Product number -
Other names N-Methyl-N'-(pyridyl-3)-harnstoff

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:39805-01-1 SDS

39805-01-1Downstream Products

39805-01-1Relevant academic research and scientific papers

INFRARED AND 1H-NMR STUDY OF MOLECULAR CONFORMATION OF SOME N,N'-ARYLALKYLUREAS

Sudha, L. V.,Sathyanarayana, D. N.

, p. 89 - 96 (2007/10/02)

The 270 MHz 1H-NMR and IR spectra of several N,N'-arylalkylureas are analyzed in terms of their conformational properties.For most systems, the -NHCONH- group adopts a less energetic trans-cis conformation which is stabilized by unsymmetric intramolecular hydrogen bonding of lower polarizability, in contrast ot other N,N'-disubstituted ureas which are predominantly found in the trans-trans form.The influence of the N-substituent on hydrogen bonding and molecular conformation is emphasized.

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