852693-74-4

Basic information

• Product Name: 3-Butenoic acid, 2-[[(1,1-diMethylethoxy)carbonyl]aMino]-, Methyl ester, (2S)-
• Synonyms: 3-Butenoic acid, 2-[[(1,1-diMethylethoxy)carbonyl]aMino]-, Methyl ester, (2S)-
• CAS NO: 852693-74-4
• Molecular Formula: C10H17NO4
• Molecular Weight: 215.24628
• Mol File: 852693-74-4.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 303.4°C at 760 mmHg
• Flash Point: 137.3°C
• Appearance: /
• Density: 1.05g/cm³
• Vapor Pressure: 0.00093mmHg at 25°C
• Refractive Index: 1.451
• PKA: 10.70±0.46(Predicted)
• CAS DataBase Reference: 3-Butenoic acid, 2-[[(1,1-diMethylethoxy)carbonyl]aMino]-, Methyl ester, (2S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Butenoic acid, 2-[[(1,1-diMethylethoxy)carbonyl]aMino]-, Methyl ester, (2S)-(852693-74-4)
• EPA Substance Registry System: 3-Butenoic acid, 2-[[(1,1-diMethylethoxy)carbonyl]aMino]-, Methyl ester, (2S)-(852693-74-4)

Safety Data

• Hazardous Substances Data: 852693-74-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H17NO4/c1-6-7(8(12)14-5)11-9(13)15-10(2,3)4/h6-7H,1H2,2-5H3,(H,11,13)/t7-/m0/s1

Upstream product

• 33900-24-2 N-(tert-butoxycarbonyl)-L-methionine methyl ester 
• 4248-19-5 tert-butyl carbazate 
• 100038-62-8 methyl 4-(phenylseleno)-2(E)-butenoate 
• 1826-67-1 vinyl magnesium bromide 
• 138219-39-3 2-bromo-2-(N-tert-butoxycarbonylamino)acetic acid methyl ester 
• 31954-27-5 N-(tert-butoxycarbonyl)glycine methyl ester 
• 24424-99-5 di-tert-butyl dicarbonate 
• 623-43-8 crotonic acid methyl ester 
• 121056-95-9 trimethyl 2-(tert-butoxycarbonylamino)phosphonoacetate 
• 63658-16-2 (Z)-methyl 2-((tertbutoxycarbonyl)amino)but-2-enoate 
• 186581-53-3 diazomethane 
• 91028-39-6 L-2-<<(tert-Butyloxy)carbonyl>amino>-3-butenoic Acid 
• 133625-87-3 tert-butyl (4S)-2,2-dimethyl-4-vinyl-1,3-oxazolidine-3-carboxylate 
• 75266-40-9 N-benzyloxycarbonyl-L-α-vinylglycine methyl ester 

Relevant articles and documents

-

-

Application of allylic amine formation from aziridine-2-ol under Appel reaction condition: Synthesis of N-(tert-butoxycarbonyl)-D-vinyl glycine methyl ester

PPh3/I2/imidazolde mediated allyl amine formation from aziridine-2-alcohol was explored for the synthesis of N-(tert-butoxycarbonyl)-D-vinyl glycine methyl ester.

Cross-metathesis of C-allyl iminosugars with alkenyl oxazolidines as a key step in the synthesis of C-iminoglycosyl α-amino acids. A route to iminosugar containing C-glycopeptides

A general access to a novel class of sugar α-amino acids composed of iminofuranose and iminopyranose residues anomerically linked to the glycinyl group through an alkyl chain is described. A set of eight compounds was prepared by the same reaction sequenc