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33024-57-6

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33024-57-6 Usage

General Description

1-cyclohex-2-en-1-yl-3-methylurea, also known as CXMU, is a chemical compound with the molecular formula C8H12N2O. It is a white crystalline solid that is soluble in water and organic solvents. CXMU is commonly used as a reagent in organic synthesis and pharmaceutical research. It is also known for its ability to form stable complexes with transition metal ions, making it useful in catalytic processes. Additionally, CXMU has been studied for its potential applications in agriculture as a plant growth regulator. However, its exact mechanisms of action and specific uses are still being explored.

Check Digit Verification of cas no

The CAS Registry Mumber 33024-57-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,0,2 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 33024-57:
(7*3)+(6*3)+(5*0)+(4*2)+(3*4)+(2*5)+(1*7)=76
76 % 10 = 6
So 33024-57-6 is a valid CAS Registry Number.

33024-57-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyclohex-2-en-1-yl-3-methylurea

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:33024-57-6 SDS

33024-57-6Relevant articles and documents

Direct amination of olefins through sequential triazolinedione ene reaction and carbanion-assisted cleavage of the N-N urazole bond

Adam, Waldemar,Pastor, Aurelia,Wirth, Thomas

, p. 1295 - 1297 (2007/10/03)

(formula presented) Allylic amines 5 are obtained in 30-55% overall yields by the base-catalyzed hydrolysis of trialkylated allylic urazoles 3; the latter are prepared by the TAD ene reaction of the appropriate olefin and further N-alkylation with α-bromo

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