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82704-14-1

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82704-14-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82704-14-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,7,0 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82704-14:
(7*8)+(6*2)+(5*7)+(4*0)+(3*4)+(2*1)+(1*4)=121
121 % 10 = 1
So 82704-14-1 is a valid CAS Registry Number.

82704-14-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-1-benzyl-N-(2-formylphenyl)pyrrolidine-2-carboxamide

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:82704-14-1 SDS

82704-14-1Relevant articles and documents

Preparation of labeled aromatic amino acids: Via late-stage18F-fluorination of chiral nickel and copper complexes

Craig, Austin,Kolks, Niklas,Urusova, Elizaveta A.,Zischler, Johannes,Brugger, Melanie,Endepols, Heike,Neumaier, Bernd,Zlatopolskiy, Boris D.

, p. 9505 - 9508 (2020/09/03)

A general protocol for the preparation of 18F-labeled AAAs and α-methyl-AAAs applying alcohol-enhanced Cu-mediated radiofluorination of Bpin-substituted chiral complexes using Ni/Cu-BPX templates as double protecting groups is reported. The chiral auxiliaries are easily accessible from commercially available starting materials in a few synthetic steps. The versatility of the method was demonstrated by the high-yielding preparation of a series of [18F]F-AAAs and the successful implementation of the protocol into automated radiosynthesis modules. This journal is

ASYMMETRIC SYNTHESIS OF THREONINE AND RETRORACEMIZATION OF AMINO ACIDS USING Ni(II) COMPLEXES OF SCHIFF BASES WITH S-2-N-(N'-BENZYLPROLYL)AMINOBENZALDEHYDE

Belokon', Yu. N.,Chernoglazova, N. I.,Kochetkov, K. A.,Garbalinskaya, N. S.,Ryzhov, M. G.,et al.

, p. 738 - 746 (2007/10/02)

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(S)-o-N-(N-Benzylprolyl)aminobenzaldehyde and (S)-o-N-(N-Benzylprolyl)aminoacetophenone as Reagents for Asymmetric Synthesis of Threonine

Belokon, Yuuri N.,Zeltzer, Irina E.,Ryzhov, Michail G.,Saporovskaya, Marina B.,Bakhmutov, Vladimir I.,Belikov, Vasili M.

, p. 180 - 181 (2007/10/02)

Chiral aldehydes and ketones, derivatives of proline and piperidine-2-carboxylic acid have been synthesized and their Schiff bases with glycine form copper complexes which were hydroxyethylated with acetaldehyde; decomposition of the complexes obtained gave threonine with an optical purity of up to 97-100percent and with threo/allo ratios of up to 19 : 1, and the chiral reagents can be recovered and reused with no loss of optical purity of the threonine.

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