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(2S,3S,3''S)-N-[3-(3-acetoxy-3-methoxycarbonylpropanamido)-3- tert-butoxycarbonylpropanoyl]azetidine-2-carboxylic Acid tert-butyl Ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

201283-56-9

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201283-56-9 Usage

Chemical Properties

White Solid

Check Digit Verification of cas no

The CAS Registry Mumber 201283-56-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,2,8 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 201283-56:
(8*2)+(7*0)+(6*1)+(5*2)+(4*8)+(3*3)+(2*5)+(1*6)=89
89 % 10 = 9
So 201283-56-9 is a valid CAS Registry Number.
InChI:InChI=1/C23H36N2O10/c1-13(26)33-16(21(31)32-8)12-17(27)24-14(19(29)34-22(2,3)4)11-18(28)25-10-9-15(25)20(30)35-23(5,6)7/h14-16H,9-12H2,1-8H3,(H,24,27)/t14-,15-,16-/m0/s1

201283-56-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3S,3''S)-N-[3-(3-acetoxy-3-methoxycarbonylpropanamido)-3-t-butoxycarbonylpropanoyl]azetidine-2-carboxylic acid t-butyl ester

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:201283-56-9 SDS

201283-56-9Relevant academic research and scientific papers

Expeditious synthesis of nicotianamine and 2′-deoxymugineic acid

Miyakoshi, Katsuhiro,Oshita, Jun,Kitahara, Takeshi

, p. 3355 - 3360 (2001)

A simple and efficient method of synthesizing nicotianamine 4 and 2′-deoxymugineic acid 3 was devised. We employed thioamide as an intermediate and the title compounds (4 and 3) were afforded via chemoselective reduction of the thioamides in 33% overall yield through 7 steps and 30% overall yield through 8 steps, respectively.

A novel synthetic approach towards phytosiderophores: Expeditious synthesis of nicotianamine and 2'-deoxymugineic acid

Klair, Sukhbinder S.,Mohan, Hindupur R.,Kitahara, Takeshi

, p. 89 - 92 (2007/10/03)

A short and a novel approach for synthesis of nicotianamine, 2'- deoxymugineic acid and related phytosiderophores has been achieved through peptide intermediates. Selective amide reduction in the presence of ester functionalities by conversion to thioamid

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