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N-butyl-3,4,5-trimethoxybenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70001-46-6

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70001-46-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70001-46-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,0,0 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 70001-46:
(7*7)+(6*0)+(5*0)+(4*0)+(3*1)+(2*4)+(1*6)=66
66 % 10 = 6
So 70001-46-6 is a valid CAS Registry Number.

70001-46-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-butyl-3,4,5-trimethoxybenzamide

1.2 Other means of identification

Product number -
Other names 3,4,5-Trimethoxybenzoylbutylamid

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:70001-46-6 SDS

70001-46-6Relevant academic research and scientific papers

In situ protection and deprotection of amines for iron catalyzed oxidative amidation of aldehydes

Bathini, Thulasiram,Rawat, Vikas S.,Bojja, Sreedhar

supporting information, p. 5656 - 5660 (2015/09/15)

An environmentally friendly synthetic route by the application of CO2 to synthesize amides via in situ protection and deprotection of amines for iron catalyzed oxidative amidation of aldehydes was developed. Various secondary and tertiary amides have been synthesized in moderate to good yields under mild and neutral reaction conditions. The use of amine hydrochloride salts and hence base for neutralization step is totally avoided in this protocol.

11a-Methano-TXA compounds

-

, (2008/06/13)

The present invention provides novel 11a-methano-TXA compounds and intermediates and processs for their preparation. Further provided are methods for using these novel TXA analogs as inhibitors of thromboxane synthetase, rendering these analogs useful for a variety of pharmacological purposes. These pharmacological uses include anti-inflammatory, anti-thromobitc, and anti-asthma indications.

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