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Benzamide, 2-(ethylamino)-4,5-dihydroxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

127793-87-7

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127793-87-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127793-87-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,7,9 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 127793-87:
(8*1)+(7*2)+(6*7)+(5*7)+(4*9)+(3*3)+(2*8)+(1*7)=167
167 % 10 = 7
So 127793-87-7 is a valid CAS Registry Number.

127793-87-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(ethylamino)-4,5-dihydroxybenzamide

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:127793-87-7 SDS

127793-87-7Downstream Products

127793-87-7Relevant academic research and scientific papers

Synthesis of 3,4-dihydroxy-6-(N-ethylamino)benzamide, a new phenolic compound isolated from green pepper (Piper nigrum L.) berries

Variyar, Prasad S.,Bandyopadhyay, Chiranjib

, p. 911 - 913 (2007/10/03)

The synthesis of 3,4-dihydroxy-6-(N-ethylamino)benzamide (9), a novel phenolic constittuent of green pepper berries, responsible for its blackening during drying process has been developed from vanillic acid (1) in eight steps.Use of mild reaction conditions such as employing anhydrous ammonium formate as hydrogen transfer agent during reduction of 3 at room temperature (Step III), reductive alkylation of 4 with sodium borohydride and acetic acid (Step IV) and protecting the amino group using acetic acid (Step IV) and protecting the amino group using trifluoroacetic acid prior to demethylation (Step VII) and hydrolysis (Step VIII) results in an acceptable yield of the final product (9) despite its highly unstable nature.

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