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52883-25-7

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52883-25-7 Usage

Type of compound

Organic compound

Type of derivative

Urea derivative

Substituent

Butoxy group attached to the nitrogen atom

Industrial applications

Solvent, intermediate in organic synthesis, component in pharmaceuticals

Physical state at room temperature

Colorless liquid

Solubility

Soluble in water and most organic solvents

Potential uses

Agricultural and cosmetic products, production of polyurethane materials

Safety precautions

Can be harmful if ingested, inhaled, or absorbed through the skin. Appropriate measures should be taken to handle this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 52883-25-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,8 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 52883-25:
(7*5)+(6*2)+(5*8)+(4*8)+(3*3)+(2*2)+(1*5)=137
137 % 10 = 7
So 52883-25-7 is a valid CAS Registry Number.

52883-25-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name butoxyurea

1.2 Other means of identification

Product number -
Other names Urea,N-butoxy

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:52883-25-7 SDS

52883-25-7Downstream Products

52883-25-7Relevant articles and documents

Geminal systems 50. Synthesis and alcoholysis of N-acyloxy-N-alkoxy derivatives of ureas, carbamates, and benzamides

Shtamburg,Klots,Pleshkova,Avramenko,Ivonin,Tsygankov,Kostyanovsky

, p. 2251 - 2260 (2007/10/03)

Procedures were developed for the synthesis of N-acyloxy-N-alkoxy derivatives of ureas, carbamates, and benzamides by the reactions of the corresponding N-alkoxy-N-chloro derivatives with sodium carboxylates in MeCN. N-Chloro-N-ethoxy-p-toluenesulfonamide was inert in this reaction. Alcoholysis of N-acyloxy-N-alkoxy derivatives of ureas, carbamates, and tert-alkylamines afforded the corresponding N,N-dialkoxy derivatives, whereas alcoholysis of N-acetoxy-N-ethoxybenzamide gave rise to alkyl benzoates.

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