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344299-89-4

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  • (2S,3S,3''S)-N-[3-(3-acetoxy-3-methoxycarbonylpropanamino)-3-tert-butoxycarbonylpropanyl]azetidine-2-carboxylic Acid tert-Butyl Ester

    Cas No: 344299-89-4

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  • (2S,3S,3''S)-N-[3-(3-acetoxy-3-methoxycarbonylpropanamino)-3-tert-butoxycarbonylpropanyl]azetidine-2-carboxylic Acid tert-Butyl Ester

    Cas No: 344299-89-4

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344299-89-4 Usage

Chemical Properties

Yellow Semi-Solid

Check Digit Verification of cas no

The CAS Registry Mumber 344299-89-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,4,2,9 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 344299-89:
(8*3)+(7*4)+(6*4)+(5*2)+(4*9)+(3*9)+(2*8)+(1*9)=174
174 % 10 = 4
So 344299-89-4 is a valid CAS Registry Number.

344299-89-4SDS

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 tert-butyl (2S)-1-[(3S)-3-[[(3S)-3-acetyloxy-4-methoxy-4-oxobutyl]amino]-4-[(2-methylpropan-2-yl)oxy]-4-oxobutyl]azetidine-2-carboxylate

1.2 Other means of identification

Product number -
Other names (2S,3S,3''S)-N-[3-(3-acetoxy-3-methoxycarbonylpropanamino)-3-tert-butoxycarbonylpropanyl]azetidine-2-carboxylic Acid tert-Butyl Ester

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:344299-89-4 SDS

344299-89-4Downstream Products

344299-89-4Relevant articles and documents

Expeditious synthesis of nicotianamine and 2′-deoxymugineic acid

Miyakoshi, Katsuhiro,Oshita, Jun,Kitahara, Takeshi

, p. 3355 - 3360 (2007/10/03)

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.

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