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5-Hexenoic acid, 2-[(phenylmethylene)amino]-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

110511-03-0

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110511-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110511-03-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,5,1 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 110511-03:
(8*1)+(7*1)+(6*0)+(5*5)+(4*1)+(3*1)+(2*0)+(1*3)=50
50 % 10 = 0
So 110511-03-0 is a valid CAS Registry Number.

110511-03-0SDS

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 methyl 2-(benzylideneamino)hex-5-enoate

1.2 Other means of identification

Product number -
Other names methyl 2-(benzylideneamino)-5-hexenoate

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:110511-03-0 SDS

110511-03-0Relevant academic research and scientific papers

Bridged (β-alkoxyalkyl)CoIII(salen) complexes by intramolecular alkoxycobaltation of unactivated alkenes: New models for coenzyme B12

Blaauw, Rolf,Kingma, Irene E.,Laan, Jan H.,Van Der Baan, Juul L.,Balt, Sijbe,De Bolster, Martinus W. G.,Klumpp, Gerhard W.,Smeets, Wilberth J. J.,Spek, Anthony L.

, p. 1199 - 1210 (2007/10/03)

CoII(salen) derivatives (salen = {N,N′-ethylenebis[salicylideneaminato]}) whose ethanediyl moiety carries an alkenyl side-chain R [R = prop-2-en-1-yl (6a), 2-methylprop-2-en-1-yl (6b), but-2-en-1-yl (6c), but-3-en-1-yl (6d)] react with oxygen a

Intramolecular Alkoxycobaltation: a Novel Route to the Cobalt-Carbon Bond in a Coenzyme B12 Model

Kingma, Irene E.,Wiersma, Marten,Baan, Juul L. van der,Balt, Sijbe,Bickelhaupt, Friedrich,et al.

, p. 832 - 834 (2007/10/02)

Co(II)(salen) derivatives whose ethanediyl moiety carries an ω-alkenyl side chain react with oxygen and methanol or ethanol to give, via interaction between intermediate Co(III) species and the pendant olefin, alkylated products with a β-alkoxy substituted carbon bridge between cobalt and the equatorial ligand; the corresponding intermolecular reaction between Co(II)(salen) and hex-1-ene does not take place.

Synthesis and Biological Properties of α-Mono- and α-Difluoromethyl Derivatives of Tryptophan and 5-Hydroxytryptophan

Schirlin, D.,Gerhart, F.,Hornsperger, J. M.,Hamon, M.,Wagner, J.,Jung, M. J.

, p. 30 - 36 (2007/10/02)

The syntheses of α-mono- amd α-difluoromethyl derivatives of tryptophan and 5-hydroxytryptophan are described.In an attempt to selectively regulate serotonin synthesis, α-(mono- and difluoromethyl)tryptophan were tested in vivo as precusors (or prodrugs)

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