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N-alpha-Benzyloxycarbonyl-L-valinyl-diazomethane, (3S)-3-Z-amino-1-diazo-4-methyl-2-pentanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90105-46-7

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90105-46-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90105-46-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,1,0 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 90105-46:
(7*9)+(6*0)+(5*1)+(4*0)+(3*5)+(2*4)+(1*6)=97
97 % 10 = 7
So 90105-46-7 is a valid CAS Registry Number.

90105-46-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Carbamic acid, N-[(1S)-3-diazo-1-(1-methylethyl)-2-oxopropyl]-, phenylmethyl ester

1.2 Other means of identification

Product number -
Other names N-alpha-Benzyloxycarbonyl-L-valinyl-diazomethane, (3S)-3-Z-amino-1-diazo-4-methyl-2-pentanone

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:90105-46-7 SDS

90105-46-7Relevant academic research and scientific papers

Continuous flow synthesis of β-amino acids from α-amino acids via Arndt-Eistert homologation

Pinho, Vagner D.,Gutmann, Bernhard,Kappe, C. Oliver

, p. 37419 - 37422 (2014/12/09)

A fully continuous four step process for the preparation of β-amino acids from their corresponding α-amino acids utilizing the Arndt-Eistert homologation approach is described. the Partner Organisations 2014.

Synthesis of enantiopure free and N-benzyloxycarbonyl-protected 3-substituted homotaurines from naturally occurring amino acids

Zheng, Yongpeng,Xu, Jiaxi

, p. 5197 - 5206 (2014/12/10)

Enantiopure N-benzyloxycarbonyl-protected and free 3-substituted homotaurines were synthesized from naturally occurring amino acids via N-benzyloxycarbonyl protection, Arndt-Eistert homologation, reduction, esterification with thioacetic acid, and oxidation with performic acid. The current method is a convenient, practical, and salt-free method for the synthesis of enantiopure 3-substituted homotaurine with moderate to good yields.

Synthesis of enantiopure free and N-benzyloxycarbonyl-protected 3-substituted homotaurines from naturally occurring amino acids

Zheng, Yongpeng,Xu, Jiaxi

, p. 5197 - 5206 (2014/07/08)

Enantiopure N-benzyloxycarbonyl-protected and free 3-substituted homotaurines were synthesized from naturally occurring amino acids via N-benzyloxycarbonyl protection, Arndt-Eistert homologation, reduction, esterification with thioacetic acid, and oxidation with performic acid. The current method is a convenient, practical, and salt-free method for the synthesis of enantiopure 3-substituted homotaurine with moderate to good yields.

Facile synthesis of optically active imidazole derivatives

Marek, Ales,Kulhanek, Jiri,Ludwig, Miroslav,Bures, Filip

, p. 1183 - 1190 (2008/02/07)

Five optically active imidazole derivatives have been synthesized via a facile 4-step reaction sequence starting from commercially available and inexpensive N-Cbz amino acids. While microwave assisted condensation was unsuccessful, the condensation of the

Total synthesis of N14-desacetoxytubulysin H

Wipf, Peter,Wang, Zhiyong

, p. 1605 - 1607 (2008/02/03)

Equation presented The N14-desacetoxy analogue of tubulysin H was prepared in 20 steps and 2.1% overall yield. Our strategy features a thiazole anion addition to assemble the tubuvaline residue at the C(10)-C(11) bond, as well as acylations at

Effective methods for the synthesis of N-methyl β-amino acids from all twenty common α-amino acids using 1,3-oxazolidin-5-ones and 1,3-oxazinan-6-ones

Hughes, Andrew B.,Sleebs, Brad E.

, p. 2611 - 2637 (2007/10/03)

N-Methyl β-amino acids are generally required for application in the synthesis of potentially bioactive modified peptides and other oligomers. Previous work highlighted the reductive cleavage of 1,3-oxazolidin-5-ones to synthesise N-methyl α-amino acids. Starting from α-amino acids, two approaches were used to prepare the corresponding N-methyl β-amino acids. First, α-amino acids were converted to N-methyl α-amino acids by the so-called '1,3-oxazolidin-5-one strategy', and these were then homologated by the Arndt-Eistert procedure to afford N-protected N-methyl β-amino acids derived from the 20 common α-amino acids. These compounds were prepared in yields of 23-57% (relative to N-methyl α-amino acid). In a second approach, twelve N-protected α-amino acids could be directly homologated by the Arndt-Eistert procedure, and the resulting β-amino acids were converted to the 1,3-oxazinan-6-ones in 30-45% yield. Finally, reductive cleavage afforded the desired N-methyl β-amino acids in 41-63% yield. One sterically congested β-amino acid, 3-methyl-3-aminobutanoic acid, did give a high yield (95%) of the 1,3-oxazinan-6-one (65), and subsequent reductive cleavage gave the corresponding AIBN-derived N-methyl β-amino acid 61 in 71% yield (Scheme 2). Thus, our protocols allow the ready preparation of all N-methyl β-amino acids derived from the 20 proteinogenic α-amino acids.

Synthesis of new β-amino acids via 5-oxazolidinones and the arndt-eistert procedure

Hughes, Andrew B.,Sleebs, Brad E.

, p. 778 - 784 (2007/10/03)

N-Methyl β-amino acids are potentially useful amino acid derivatives for incorporation in lead peptide therapeutics. The syntheses of five such compounds are presented. Their synthesis via 6-oxazinanones was low yielding. Alternatively, reductive cleavage of a 5-oxazolidinone gave the N-methyl β-amino acid, which was then homologated via an Arndt-Eistert procedure in high yield to give the N-methyl α-amino acid. CSIRO 2005.

Chiral imidazole derivatives synthesis from enantiopure N-protected α-amino acids

Bures, Filip,Kulhanek, Jiri

, p. 1347 - 1354 (2007/10/03)

A route to the preparation of enantiopure ligands based on a 2-phenylimidazol ring is described. The stereogenic centre is placed into the chain bonded to the fourth carbon of the imidazole ring. The synthesis starts from inexpensive and readily available

Synthesis of ketomethylene amino pseudopeptide analogues via reductive amination of glyoxals derived from α-amino acids

Groarke, Michelle,Hartzoulakis, Basil,McKervey, M. Anthony,Walker, Brian,Williams, Carvell H.

, p. 153 - 155 (2007/10/03)

The reductive amination of an amino acid derived glyoxal, with the free amino group of a protected amino acid or oligopeptide fragment, has been developed as a simple and efficient method for the preparation of ketomethylene amino pseudooligopeptide isost

Synthesis of optically active β-amino acid N-carboxyanhydrides

Cheng, Jianjun,Ziller, Joseph W.,Deming, Timothy J.

, p. 1943 - 1946 (2007/10/03)

(Equation presented) Methodology has been developed for the general synthesis of optically active β-amino acid N-carboxyanhydrides (β-NCAs) through cyclization of Nβ-Boc or Nβ-Cbz β-amino acids using phosphorus tribromide. The format

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