57294-38-9

Basic information

• Product Name: BOC-GAMMA-ABU-OH
• Synonyms: NALPHA-tert-Butoxycarbonyl-4-aminobutyric acid;N-t-Butyloxycarbonyl-gamma-aminobutyric acid, Boc-4-Abu-OH;Boc--aminobutyric acid (Boc-GABA);N-Boc-γ-aminobutyric acid, 98+%;Butanoic acid,4-[[(1,1-dimethylethoxy)carbonyl]amino]-;4-(Boc-amino)butyric acid, Boc-GABA;γ-(Boc-amino)butyric acid, 4-(tert-Butoxycarbonylamino)butyric acid, Boc-GABA;4-[(tert-Butyloxycarbonyl)amino]butanoic acid
• CAS NO: 57294-38-9
• Molecular Formula: C₉H₁₇NO₄
• Molecular Weight: 203.24
• EINECS: 1533716-785-6
• Product Categories: Amino Acids;Boc-Amino Acids and Derivative;Unusual Amino Acids
• Mol File: 57294-38-9.mol
• Article Data: 2

Chemical Properties

• Melting Point: 55-59 °C
• Boiling Point: 78-82 °C0.2 mm Hg(lit.)
• Flash Point: >230 °F
• Appearance: White to off-white/Powder
• Density: 1.1886 (rough estimate)
• Vapor Pressure: 4.4E-06mmHg at 25°C
• Refractive Index: 1.4315 (estimate)
• Storage Temp.: 2-8°C
• Solubility: soluble in Methanol
• PKA: 4.70±0.10(Predicted)
• BRN: 1869578
• CAS DataBase Reference: BOC-GAMMA-ABU-OH(CAS DataBase Reference)
• NIST Chemistry Reference: BOC-GAMMA-ABU-OH(57294-38-9)
• EPA Substance Registry System: BOC-GAMMA-ABU-OH(57294-38-9)

Safety Data

• Hazard Codes: Xi
• Statements: 44-36/37/38-22
• Safety Statements: 37/39-26-24/25
• WGK Germany: 3
• F: 10-21
• HazardClass: IRRITANT
• Hazardous Substances Data: 57294-38-9(Hazardous Substances Data)

Usage

Chemical Properties

White crystalline powder

Uses

N-Boc-gamma-aminobutyric Acid is used in the preparation of isopropyl-methylcyclohexyl aminobutyrate as a potential anticonvulsant.

InChI:InChI=1/C9H17NO4/c1-9(2,3)14-8(13)10-6-4-5-7(11)12/h4-6H2,1-3H3,(H,10,13)(H,11,12)/p-1

Upstream product

• 1355024-10-0 t-butyl 3-(((perylen-3-yl)methoxy)carbonyl)propylcarbamate 
• 86953-79-9 tert-butyl pyrrolidine-1-carboxylate 

Downstream Products

• 161451-66-7 [3-(3-Benzyloxycarbonylamino-propylcarbamoyl)-propyl]-carbamic acid tert-butyl ester 
• 94897-10-6 tert-butyl 4-(4-(2-(diethylamino)ethylcarbamoyl)phenylaminooxy)-4-oxobutylcarbamate 
• 123642-54-6 (4,5-dimethoxy-2-nitrophenyl)methyl 4butanoate 
• 102537-72-4 (3-{[4-(2-Benzoyl-4-chloro-phenyl)-5-methyl-4H-[1,2,4]triazol-3-ylmethyl]-carbamoyl}-propyl)-carbamic acid tert-butyl ester 
• 95647-72-6 (3-{2-[(1R,2R)-2-(2,6-Dihydroxy-4-pentyl-phenyl)-4-methyl-cyclohex-3-enyl]-allylcarbamoyl}-propyl)-carbamic acid tert-butyl ester 
• 94111-77-0 trans-5--15-phenyl>-2,8,12,18-tetraethyl-3,7,13,17-tetramethylporphyrin 
• 75178-87-9 (4-hydroxybutyl)carbamic acid tert-butyl ester 
• 150311-77-6 4-(t-butoxycarbamoyl)-N-(4'-dimethylaminophenyl)butanamide 
• 154656-95-8 N-tert-butyloxycarbonyl-γ-aminobutyric acid N',N'-dimethylamide 
• 94994-39-5 4-[(tert-butoxycarbonyl)(methyl)amino]butanoic acid 
• 158690-75-6 4-tert-Butoxycarbonylamino-butyric acid tert-butoxycarbonyl-(2-nitro-phenyl)-methyl ester 
• 1026967-39-4 (S)-2-{(S)-2-[(S)-2-(4-tert-Butoxycarbonylamino-butyrylamino)-3-phenyl-propionylamino]-4-methyl-pentanoylamino}-3-phenyl-propionic acid methyl ester 
• 168017-78-5 {3-[3-(3-Piperidin-1-ylmethyl-phenoxy)-propylcarbamoyl]-propyl}-carbamic acid tert-butyl ester 
• 187996-52-7 N-tert-butoxycarbonyl-γ-aminobutyric acid pentafluorophenyl ester 

Relevant articles and documents

PHOTOLYTIC COMPOUNDS AND TRIPLET-TRIPLET ANNIHILATION MEDIATED PHOTOLYSIS

The invention provides novel photolytic compounds and prodrugs, nanoparticles and compositions thereof, and methods of conducting photolysis mediated by triplet-triplet annihilation.