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62413-47-2

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62413-47-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62413-47-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,1 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62413-47:
(7*6)+(6*2)+(5*4)+(4*1)+(3*3)+(2*4)+(1*7)=102
102 % 10 = 2
So 62413-47-2 is a valid CAS Registry Number.

62413-47-2SDS

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 (2R,3E)-4-phenyl-3-buten-2-ol

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:62413-47-2 SDS

62413-47-2Relevant articles and documents

Regio- and stereoselective reduction of trans-4-phenylbut-3-en-2-one using carrot, celeriac, and beetroot enzyme systems in an organic solvent

Majewska, Ewa,Koz?owska, Mariola

, p. 6331 - 6332 (2013)

(S)-trans-4-Phenylbut-3-en-2-ol has been obtained in excellent yields and with high enantiomeric excess in the reduction of trans-4-phenylbut-3-en-2-one using the comminuted roots of carrot (Daucus carota L.), celeriac (Apium graveolens L. var. rapaceum),

Self-Assembling All-Enzyme Hydrogels for Flow Biocatalysis

Peschke, Theo,Bitterwolf, Patrick,Gallus, Sabrina,Hu, Yong,Oelschlaeger, Claude,Willenbacher, Norbert,Rabe, Kersten S.,Niemeyer, Christof M.

, p. 17028 - 17032 (2018)

Continuous flow biocatalysis is an emerging field of industrial biotechnology that uses enzymes immobilized in flow channels for the production of value-added chemicals. We describe the construction of self-assembling all-enzyme hydrogels that are compris

Dramatic titanium alkoxide effect in the catalytic enantioselective addition of dialkylzincs to aldehydes

Nowotny, Stefan,Vettel, Stephan,Knochel, Paul

, p. 4539 - 4540 (1994)

The use of Ti(Ot-Bu)4, or related bulky titanium (IV) alkoxides, as cocatalysts instead of Ti(Oi-Pr)4 in the enantioselective addition of dimethylzinc to aldehydes in the prescence of the catalyst 2 (8 mol%) leads to a dramatic impro

Nickel-Catalyzed Enantioselective Hydroboration of Vinylarenes

Tran, Hai N.,Stanley, Levi M.

supporting information, p. 395 - 399 (2021/12/27)

The enantioselective hydroboration of vinylarenes catalyzed by a chiral, nonracemic nickel catalyst is presented as a facile method for generating chiral benzylic boronate esters. Various vinylarenes react with bis(pinacolato)diboron (B2pin2) in the presence of MeOH as a hydride source to form chiral boronate esters in up to 92% yield with up to 94% ee. The use of anhydrous Me4NF to activate B2pin2 is crucial for ensuring fast transmetalation to achieve high enantioselectivities.

Manganese catalyzed enantio- and regioselective hydrogenation of α,β-unsaturated ketones using an imidazole-based chiral PNN tridentate ligand

Wang, Ze,Zhao, Xianghua,Huang, An,Yang, Zehui,Cheng, Yuqi,Chen, Jiachen,Ling, Fei,Zhong, Weihui

supporting information, (2021/09/22)

The enantioselective 1,2-reduction of α,β-unsaturated ketones has been achieved using a chiral pincer Mn catalyst. A series of PNN tridentate ligands containing benzimidazole groups were designed with ferrocene as the backbone, which coordinated with Mn t

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