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2-Propenoic acid, 3-[(1-oxo-2-propenyl)amino]phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35289-74-8

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35289-74-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35289-74-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,2,8 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 35289-74:
(7*3)+(6*5)+(5*2)+(4*8)+(3*9)+(2*7)+(1*4)=138
138 % 10 = 8
So 35289-74-8 is a valid CAS Registry Number.

35289-74-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-(prop-2-enoylamino)phenyl] prop-2-enoate

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:35289-74-8 SDS

35289-74-8Downstream Products

35289-74-8Relevant academic research and scientific papers

Surface-emitting semiconductor laser

-

, (2007/10/13)

A surface-emitting type semiconductor laser includes: a first mirror (102); an active layer (103) formed above the first mirror (102); a second mirror (104) formed above the active layer (103); and a current constricting section (105) formed above or below the active layer (103), wherein the second mirror (104) has a plurality of concave sections (111) arranged within a plane perpendicular to a light emission direction, and a light confining region (110) surrounded by the concave sections (111) is formed inside a region surrounded by the current constricting section (105) as viewed in a plan view.

3-substituted anilines as scaffolds for the construction of glutamine synthetase and DXP-reductoisomerase inhibitors

Mutorwa, Marius,Salisu, Sheriff,Blatch, Gregory L.,Kenyon, Colin,Kaye, Perry T.

experimental part, p. 2723 - 2736 (2009/12/09)

Access to a series of truncated ATP analogs, as potential anti-tuberculosis agents, has been explored via alkylation and acylation of 3-aminophenol, whereas chloroacetylation, using chloroacetyl chloride, and subsequent Arbuzov phosphonation of a series of 3-substituted anilines have afforded a series of phosphonate derivatives as potential antimalarial agents.

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