ChemicalBook Product Catalog Biochemical Engineering Amino Acids and Derivatives Alanine derivatives Boc-beta-alanine

Boc-beta-alanine

Boc-beta-alanine Basic information
Product Name:Boc-beta-alanine
Synonyms:N-T-BOC-BETA-ALANINE;N-TERT-BOC-BETA-ALANINE;N-T-BUTOXYCARBONYL-BETA-ALANINE;N-TERT-BUTOXYCARBONYL-BETA-ALANINE;N-ALPHA-TERT-BUTYLOXYCARBONYL-BETA-ALANINE;BOC-SS-AAL-OH;N-Boc-β-alanine, 99%;N-(tert-Butyloxycarbonyl)-β-alanine
CAS:3303-84-2
MF:C8H15NO4
MW:189.21
EINECS:221-979-2
Product Categories:β-Alanine [β-Ala];Boc-Amino Acids and Derivative;Boc-Amino acid series;Amino Acids;Morpholines/Thiomorpholines;Amino Acid Derivatives
Mol File:3303-84-2.mol
Boc-beta-alanine Structure
Boc-beta-alanine Chemical Properties
Melting point 76-78 °C
Boiling point 333.9±25.0 °C(Predicted)
density 1.129±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility DMSO (Slightly), Methanol (Slightly)
pka4.46±0.10(Predicted)
form Crystalline Powder
color White to off-white
BRN 1909986
InChIKeyWCFJUSRQHZPVKY-UHFFFAOYSA-N
CAS DataBase Reference3303-84-2(CAS DataBase Reference)
Safety Information
Hazard Codes Xn
Risk Statements 20/21/22-36/37/38
Safety Statements 22-24/25-36-26
WGK Germany 3
HazardClass IRRITANT
HS Code 29241990
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
Boc-beta-alanine Usage And Synthesis
DescriptionBoc-beta-Ala-OH is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. The compound can be used as a PROTAC linker in the synthesis of PROTACs. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine.
Chemical PropertiesWhite solid
UsesBoc-?β-?Ala-?OH is a reagent used in the synthesis of quinazolines as platelet aggregation inhibitors and ligands of integrin.
Boc-beta-alanine Preparation Products And Raw materials
Preparation Products(3-OXO-PROPYL)-CARBAMIC ACID TERT-BUTYL ESTER-->Propanamide, 3-amino-N-2-pyridinyl--->Carbamic acid, [3-[(2-hydroxyphenyl)amino]-3-oxopropyl]-, 1,1-dimethylethyl ester (9CI)-->Carbamic acid, N-[3-(4-methyl-1-piperazinyl)-3-oxopropyl]-, 1,1-dimethylethyl ester-->Carbamic acid, N-[3-oxo-3-(1-piperazinyl)propyl]-, 1,1-dimethylethyl ester-->propan-2-yl 3-aminopropanoate hydrochloride-->tert-butyl 3-(2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-yl)-3-oxopropylcarbamate-->3-BroMo-2,4-dioxo-piperidine-1-carboxylic acid tert-butyl ester-->Benzyl 3-(Boc-amino)propanoate
BOC-BETA-ALANINE-OSU,N-BETA-T-BOC-BETA-ALANINE N-HYDROXYSUCCINIMIDE ESTER,BOC-BETA-ALANINE N-HYDROXYSUCCINIMIDE ESTER,BOC-BETA-ALANINE HYDROXYSUCCINIMIDE ESTER Phenprobamate N-Boc-beta-alanine-beta-4'-fluorophenyl-N- BOC-ASP(OBZL)-ONP Ethyl 2-(Chlorosulfonyl)acetate Ascoric Acid BOC-(2R,3R)-3-AMINO-2-HYDROXY-5-METHYLHEXANOIC ACID EC 2.6.1.2 BOC-ASP(OCPENT)-OH N-BOC-BETA-ALANINE-BETA-4'-BROMOPHENYL-N-CARBOXYANHYDRIDE N-BOC-BETA-ALANINE-BETA-2'-CHLOROPHENYL-N-CARBOXYANHYDRIDE N-Boc-beta-alanine-beta-2'-chlorophenyl-N- L-Alanine Boc-Asp-OtBu BOC-BETA-ALANINE 4-NITROPHENYL ESTER Boc-Asp-OH Boc-Asp(Ochx)-OH (2S,3R)-3-(BOC-AMINO)-2-HYDROXY-4-(4-NITROPHENYL)BUTYRIC ACID
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