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7433-46-7

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7433-46-7 Usage

Type of compound

Organic

Functional groups

Hydroxyl group, methyl group, urea molecule

Uses

+ Reactant in organic synthesis
+ Building block in pharmaceutical and agrochemical production
+ Stabilizer
+ Formulation of personal care products

Properties

+ Water-soluble
+ Ability to form stable complexes with metal ions
+ Relative stability under normal conditions

Check Digit Verification of cas no

The CAS Registry Mumber 7433-46-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,3 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7433-46:
(6*7)+(5*4)+(4*3)+(3*3)+(2*4)+(1*6)=97
97 % 10 = 7
So 7433-46-7 is a valid CAS Registry Number.
InChI:InChI=1/C2H6N2O2/c1-3-2(5)4-6/h6H,1H3,(H2,3,4,5)

7433-46-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hydroxy-3-methylurea

1.2 Other means of identification

Product number -
Other names N-Hydroxy-N'-methyl-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:7433-46-7 SDS

7433-46-7Relevant articles and documents

MECHANISM OF THE CARBAMOYLATION OF OXIMES

Tashchi, V. P.,Rukasov, A. F.,Orlova, T. I.,Ivanov, A. P.,Tashchi, O. A.,et al.

, p. 899 - 907 (2007/10/02)

N-Acylnitrones are formed initially during the cabamoylation of oximes of the aldehydes and ketone series.Depending on the structure of the initial compounds they can then either rearrange to O-carbamoylated oximes or undergo decomposition to N-hydroxyureas and the corresponding aldehydes and ketones.In some cases isomerization of the oximes is observed under the influence of isocyanate.

N-substituted N'-hydroxythioureas.

Clifton,Bryant,Skinner

, p. 377 - 379 (2007/10/10)

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