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2,3-Butanediamine, N,N'-bis[(1S)-1-phenylethyl]-, (2R,3R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

648909-47-1

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648909-47-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 648909-47-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,8,9,0 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 648909-47:
(8*6)+(7*4)+(6*8)+(5*9)+(4*0)+(3*9)+(2*4)+(1*7)=211
211 % 10 = 1
So 648909-47-1 is a valid CAS Registry Number.

648909-47-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,3R)-2-N,3-N-bis[(1S)-1-phenylethyl]butane-2,3-diamine

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:648909-47-1 SDS

648909-47-1Downstream Products

648909-47-1Relevant academic research and scientific papers

An efficient synthetic approach towards a single diastereomer of (2R,3R)-N 2,N 3-bis((S)-1-phenylethyl)butane-2,3-diamine via metalation and demetalation

Cho, Juhyun,Nayab, Saira,Jeong, Jong Hwa

, p. 9 - 17 (2019/09/03)

Abstract: A facile synthetic approach has been adopted towards the synthesis of (2R,3R)-N2,N3-bis((S)-1-phenylethyl)butane-2,3-diamine via demetalation of its dichloro Zn(II) complex, which itself was separated from a mixture of dias

Titanium(IV)(salen) and yanadium(V)(salen) complexes derived from C 2- and C1-symmetric diamines for asymmetric cyanohydrin synthesis

Belokon', Yuri N.,Hunt, Jamie,North, Michael

scheme or table, p. 2150 - 2154 (2009/05/07)

Titanium and vanadium salen complexes have been prepared from C 2- and C1-symmetric acyclic diamines. All of the complexes catalysed the asymmetric addition of trimethylsilyl cyanide to benzaldehyde and the sense of asymmetric induction was determined by the nature of the substituents. The vanadium complex of a valine-derived diamine gave good results with a range of aromatic and aliphatic aldehydes. Georg Thieme Verlag Stuttgart.

A new chiral masked form of glyoxal diimine

Martelli, Gianluca,Savoia, Diego

, p. 1531 - 1540 (2007/10/03)

(3R,4R,5R,6R)-3,6-Diphenyl-N,N′-bis[(S)-1-phenylethyl]octa-1, 7-diene-4,5-diamine, by treatment with organolithium reagents RLi in controlled experimental conditions, underwent rearrangement and/or substitution of one or two branched allyl(s) by the R group(s). Hence, this diene behaves as a masked form of the chiral glyoxal diimine from that it is prepared, allowing the preparation of C1-symmetric 1,2-disubstituted 1,2-diamines, which are generally not available by the direct addition of organometallic reagents to the diimine, and C2-symmetric 1,2-diamines with good diastereoselectivities.

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