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28272-96-0

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28272-96-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28272-96-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,7 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 28272-96:
(7*2)+(6*8)+(5*2)+(4*7)+(3*2)+(2*9)+(1*6)=130
130 % 10 = 0
So 28272-96-0 is a valid CAS Registry Number.

28272-96-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethenylbenzaldehyde

1.2 Other means of identification

Product number -
Other names styrene-2-carboxaldehyde

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:28272-96-0 SDS

28272-96-0Relevant articles and documents

Construction of 4-Isochromanones through Cu(OTf)2-Catalysed Sequential C=O and C–O Bond Formation

Xing, Siyang,Gu, Nan,Qin, Jiajing,Cui, Hong,Li, Yan,Wang, Kui,Tian, Dawei,Chen, Bo,Yu, Guo

, p. 926 - 931 (2018)

A new strategy for the facile and efficient synthesis of 4-isochromanones has been developed. The reaction involves a Cu(OTf)2-catalysed sequential reaction of epoxides carrying electron-deficient alkenes using the solvent DMSO as the oxidant.

Diastereoselective Synthesis of the ABCD Ring System of Rubriflordilactone B

Roth, Hudson G.,Nicewicz, David A.

supporting information, p. 48 - 51 (2021/11/09)

A novel nine-step diastereoselective route to the ABCD ring system of the natural product rubriflordilactone B is reported. Use of an α-substituted butenolide derived from maleic anhydride facilitated a 1,4-conjugate addition to provide a diene. The order in which a ringclosing metathesis and enolate oxidation were performed on this compound dictated the relative stereochemistry of the target. The final product exhibited anisotropic effects during roomerature NMR studies, requiring elevatederature experiments to confirm its identity.

Enantioselective synthesis of 1-aminoindene derivativesviaasymmetric Br?nsted acid catalysis

Ding, Du,Jiang, Hua-Jie,Wang, Tao,Wu, Xiang,Zhang, Ying,Zhao, Li-Ping

supporting information, p. 9680 - 9683 (2021/09/30)

We describe a catalytic asymmetric iminium ion cyclization reaction of simple 2-alkenylbenzaldimines using a BINOL-derived chiralN-triflyl phosphoramide. The corresponding 1-aminoindenes and tetracyclic 1-aminoindanes are formed in good yields and high enantioselectivities. Further, the chemical utility of the obtained enantiopure 1-aminoindene is demonstrated for the asymmetric synthesis of (S)-rasagiline.

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