tert-Butyl carbazate

tert-Butyl carbazate Basic information
Product Name:tert-Butyl carbazate
Synonyms:TERT-BUTOXYCARBONYLHYDRAZINE;TERT-BOC-HYDRAZIDE;TERT-BUTYLOXYCARBAZATE;T-BUTOXYCARBONYL HYDRAZIDE;T-BUTYLOXYCARBONYL-HYDRAZIDE;tert-Butyl hydrazinocarboxylate;tert-Butylcarbazate,98+%;BOC-HYDRAZIDE 98%
CAS:870-46-2
MF:C5H12N2O2
MW:132.16
EINECS:212-795-3
Product Categories:bc0001;870-46-2
Mol File:870-46-2.mol
tert-Butyl carbazate Structure
tert-Butyl carbazate Chemical Properties
Melting point 39-42 °C (lit.)
Boiling point 63-65 °C/0.1 mmHg (lit.)
density 1.02
refractive index 1.4496 (estimate)
Fp 197 °F
storage temp. Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
solubility Soluble in ethanol and methanol.
pka10.74±0.20(Predicted)
form Crystalline Lumps
color White to slightly yellow
Sensitive Moisture Sensitive
BRN 1756967
InChIKeyDKACXUFSLUYRFU-UHFFFAOYSA-N
CAS DataBase Reference870-46-2(CAS DataBase Reference)
EPA Substance Registry SystemHydrazinecarboxylic acid, 1,1-dimethylethyl ester (870-46-2)
Safety Information
Hazard Codes T-F,T,F
Risk Statements 48-36/37/38-24/25-11
Safety Statements 45-36/37/39-16-24/25
RIDADR 1325
WGK Germany 3
21
TSCA Yes
HazardClass 4.1
PackingGroup III
HS Code 29280090
MSDS Information
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tert-Butyl carbazate Usage And Synthesis
Chemical PropertiesWhite to pale yellow lumps
UsesStarting material for preparing BOC-azide, a reagent to introduce the BOC amino protection.
Usestert-Butyl carbazate is used in a palladium-catalyzed cross-coupling with vinyl halides to prepare N-Boc-N-alkenylhydrazines. It is utilized in solid phase peptide synthesis and in the optical purity determination of alfa-amino aldehyde. It reacts with aldehydes to get hydrazones, which finds application as an intermediate in the synthesis of HIV-1 protease inhibitors. In addition to this, it is used as a starting material for the preparation of BOC-azide, sulfonic and carboxylic hydrazides.
Synthesis Reference(s)Journal of the American Chemical Society, 82, p. 2725, 1960 DOI: 10.1021/ja01496a018
Chemical and Pharmaceutical Bulletin, 18, p. 217, 1970 DOI: 10.1248/cpb.18.217
Purification MethodsDistil it in a Claisen flask with a water or oil bath at ca 80o. After a couple of drops have distilled, the carbazate is collected as an oil which solidifies to a snow white solid. It can be crystallised with 90% recovery from a 1:1 mixture of pet ether (b 30-60o) and pet ether (b 60-70o). [Carpino et al. Org Synth Coll Vol V 166 1973, Caprino et al. Org Synth 44 20 1964, Beilstein 3 IV 175.]
3-AMINO-1-[(1,1-DIMETHYLETHOXY)CARBONYL]-3-PIPERIDINEACETIC ACID METHYL ESTER tert-butyl 6-hydroxy-3-azabicyclo[3.1.0]hexane-3-carboxylate tert-butyl 4-oxohexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate tert-Butyl 3,8-diazabicyclo[3.2.1]octane-8-carboxylate hydrochloride 2-OXO-2,5-DIHYDRO-PYRROLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER 8-BOC-3,8-DIAZA-BICYCLO[3.2.1]OCTANE TERT-BUTYL 5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-3,6-DIHYDROPYRIDINE-1(2H)-CARBOXYLATE tert-butyl 2-oxo-6-azaspiro[3.5]nonane-6-carboxylate 1-Oxa-7-azaspiro[4.5]decane-7-carboxylic acid, 3-oxo-, 1,1-diMethylethyl ester BOC-GUANIDINE tert-Butyl L-valinate tert-Butyl acrylate t-butyl chloroformate Cyhalofop-butyl Buprofezin antioxidant 1024 DI-TERT-BUTYL ETHER 1-MENTHHYDRAZIDE

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