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1-Butanol, 3-methyl-2-[[(1S)-1-phenyl-3-butenyl]amino]-, (2S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

154228-41-8

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154228-41-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154228-41-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,2,2 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 154228-41:
(8*1)+(7*5)+(6*4)+(5*2)+(4*2)+(3*8)+(2*4)+(1*1)=118
118 % 10 = 8
So 154228-41-8 is a valid CAS Registry Number.

154228-41-8SDS

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 (2S)-3-methyl-2-[[(1S)-1-phenylbut-3-enyl]amino]butan-1-ol

1.2 Other means of identification

Product number -
Other names (2S)-3-methyl-2-((1S)-1-phenylbut-3-enylamino)butan-1-ol

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:154228-41-8 SDS

154228-41-8Relevant articles and documents

Asymmetric synthesis of δ-substituted α,β-unsaturated δ-lactams by ring closing metathesis of enantiomerically pure N-acryloyl-homoallylic amines

Fiorelli, Claudio,Savoia, Diego

, p. 6022 - 6028 (2008/02/10)

(Chemical Equation Presented) Optically pure secondary homoallylic amines, obtained by highly diastereoselective addition of allylmetal reagents to imines derived from chiral amines, were N-dealkylated, and the primary amines were converted to N-acryloyl

New utilizations of optically active homoallylamines: Highly stereoselective synthesis of cyclic guanidine and thiourea

Yanada, Reiko,Kaieda, Akira,Yanada, Kazuo,Takemoto, Yoshiji

, p. 101 - 106 (2007/10/03)

Halocyclizations of optically active homoallylguanidine and homoallylthiourea were examined. These reactions proceeded stereoselectively to give six membered cyclic guanidines and thiourea. High 1,3-asymmetric induction by the homoallylic substituents is

Aluminum-controlled reactivity and diastereoselectivity toward radical reactions of optically active aldimines with metallic samarium

Yanada,Okaniwa,Kaieda,Ibuka,Takemoto

, p. 1283 - 1286 (2007/10/03)

The intermolecular pinacol-type coupling reaction and allylation reaction of optically active imines bearing a β-hydroxy group were performed stereoselectively with metallic samarium after treatment of the imines with trimethylaluminum.

Diastereoselective allylation and alkylation of optically active imines with metallic samarium and a catalytic amount of iodine

Yanada, Reiko,Negoro, Nobuyuki,Okaniwa, Masanori,Ibuka, Toshiro

, p. 13947 - 13956 (2007/10/03)

Barbier-type allylation and alkylation of optically active imines such as N-benzylidenevalinol methyl ether was performed with metallic samarium, a catalytic amount of iodine, and allyl or alkyl halides. This reaction proceeded in a highly diastereoselect

Diastereoselective allylation of optically active imines with metallic samarium

Negoro, Nobuyuki,Yanada, Reiko,Okaniwa, Masanori,Yanada, Kazuo,Fujita, Tetsuro

, p. 835 - 836 (2007/10/03)

Barbier-type allylation of optically active imines such as N-benzylidenevalinol methyl ether was performed with metallic samarium, a catalytic amount of iodine, and allyl bromide. This reaction proceeded in a highly diastereoselective manner in THF at roo

Enantioselective Synthesis of Homoallylic Amines by Addition of Allylmetal Reagents to Imines Derived from (S)-Valine Esters

Basile, Tiziana,Bocoum, Allaye,Savoia, Diego,Umani-Ronchi, Achille

, p. 7766 - 7773 (2007/10/02)

Grignard and Barbier procedures have been applied to the addition of allylmethal (Zn, Cu, Pb, Bi, Al, In) species to imines derived from (S)-valine esters, principally the methyl ester.The Zn-mediated, CeCl3- or SnCl2-catalyzed "Barbier" reactions of the

Enantioselective Synthesis of Homoallylic Amines. Evidence of Reversible Addition of Allylzinc Bromide to Aromatic Imines Derived from (S)-Valine Methyl Ester and (S)-Valinol

Bocoum, Allaye,Savoia, Diego,Umani-Ronchi, Achille

, p. 1542 - 1544 (2007/10/02)

The reaction of aromatic and aliphatic imines derived from (S)-valine methyl ester and (S)-valinol with allyl bromide and zinc in tetrahydrofuran affords homoallylic amines with up to 100percent diastereoisomeric excess (d.e.), but in the case of the arom

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