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N-butyl-N-carbamoylbutanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73025-03-3

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73025-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73025-03-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,0,2 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73025-03:
(7*7)+(6*3)+(5*0)+(4*2)+(3*5)+(2*0)+(1*3)=93
93 % 10 = 3
So 73025-03-3 is a valid CAS Registry Number.

73025-03-3SDS

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 N-butyl-N-carbamoylbutanamide

1.2 Other means of identification

Product number -
Other names N-Butyryl-N-butyl-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:73025-03-3 SDS

73025-03-3Downstream Products

73025-03-3Relevant academic research and scientific papers

The anticonvulsant and CNS activity of N-butyryl-N-butylurea in mice

Dar,Zirvi,Fakouhi

, p. 936 - 944 (2007/10/14)

As a further extension of the authors' studies related to CNS activity of substituted butylureas, a number of derivatives of butylurea were synthesized. Among these a derivative of n-butylurea, N-butyryl-N-butylurea (NBNB) was prepared by acylation of n-butylurea with butyryl chloride in pyridine. The compound was found to possess considerable sedative-hypnotic action. Sleeping time of pentobarbital and barbital was significantly potentiated by NBNB. The compound also exhibited moderate anti-tremorine action and produced significant reduction in the activity ratio for Treadmill experiments. Significant anticonvulsive activity of NBNB was observed against strychnine, pentetrazole and supramaximal electroshock-induced convulsions. In addition to projection against tonic convulsions, the animals were also protected against strychnine and pentetrazole lethality.

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