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N-(tert-Butoxycarbonyl)-L-valinol_Molecular_structure_CAS_79069-14-0)
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N-(tert-Butoxycarbonyl)-L-valinol

Catalog No. 444413 Name Sigma Aldrich
CAS Number 79069-14-0 Website http://www.sigmaaldrich.com
M. F. C10H21NO3 Telephone 1-800-521-8956
M. W. 203.27864 Fax
Purity 96% Email
Storage Chembase ID: 146377

SYNONYMS

Title
N-(叔丁氧基羰基)-L-缬氨醇
IUPAC name
tert-butyl N-[(2S)-1-hydroxy-3-methylbutan-2-yl]carbamate
IUPAC Traditional name
tert-butyl N-[(2S)-1-hydroxy-3-methylbutan-2-yl]carbamate

DATABASE IDS

MDL Number MFCD00082635
PubChem SID 24868123
CAS Number 79069-14-0

PROPERTIES

Linear Formula (CH3)2CHCH[NHCO2C(CH3)3]CH2OH
Purity 96%
Boiling Point 208 °C(lit.)
Density 0.995 g/mL at 25 °C(lit.)
Flash Point 85 °C
Flash Point 185 °F
Optical Rotation [α]23/D -23°, c = 1 in chloroform
Refractive Index n20/D 1.449(lit.)
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26-36
German water hazard class 3

DETAILS

Description (English)
Application
Starting material for the synthesis of enantiopure homo-β-amino acids.1,2 Used in the efficient synthesis of enantiopure tetrahydroisoquinolines.3 Intermediate in the one-pot conversion of amino acid carbamates to N-derivatized 2-oxazolidinones.4
Packaging
1, 5 g in glass bottle
Description (简体中文)
Application
合成对映纯β-高氨基酸的原料。1,2用于对映纯四氢异喹啉的高效合成。3一锅法将氨基酸氨基甲酸酯转化为 N-衍生 2-噁唑烷酮的中间体。4
包装
1, 5 g in glass bottle

REFERENCES