Substance
ID:333177
Names and Identifiers
IUPAC name
3-tert-butyl 4-methyl (4S)-2,2-dimethyl-1,3-oxazolidine-3,4-dicarboxylate
IUPAC Traditional name
3-tert-butyl 4-methyl (4S)-2,2-dimethyl-1,3-oxazolidine-3,4-dicarboxylate
Synonyms
(S)-(-)-3-(叔丁氧羰基)-2,2-二甲基-4-噁唑啉羧酸甲酯Methyl (S)-(-)-3-(tert-butoxycarbonyl)-2,2-dimethyl-4-oxazolidinecarboxylateMethyl (S)-(-)-3-Boc-2,2-dimethyl-4-oxazolidinecarboxylate(S)-(-)-3-Boc-2,2-二甲基-4-噁唑啉羧酸甲酯
Properties
Product Information
Purity
98%
Optical Purity
ee: 99% (HPLC)
Empirical Formula (Hill Notation)
C12H21NO5
Physical Property
Refractive Index
n20/D 1.443(lit.)
Boiling Point
101-102 °C/2 mmHg(lit.)
Flash Point
93 °C
199.4 °F
Optical Rotation
[α]20/D -55°, c = 1.3 in chloroform
Density
1.082 g/mL at 25 °C(lit.)
Safety Information
GHS Hazard statements
H315-H319-H335
Safety Statements
26-36
German water hazard class
3
GHS Precautionary statements
P261-P305+P351+P338
European Hazard Symbols
Irritant (Xi)GHS Signal Word
Warning
MSDS Link
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Risk Statements
36/37/38
Personal Protective Equipment
Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
Molecule Details
Packaging
1, 5 g in glass bottle
Application
Precursor to a configurationally stable serinal derivative (Garner′s aldehyde) that has been used to make azasugars, sphingolipids, and the amino sugar found in calicheamicin, a potent antitumor agent.1,2,3,4,5
1, 5 g in glass bottle
Application
Precursor to a configurationally stable serinal derivative (Garner′s aldehyde) that has been used to make azasugars, sphingolipids, and the amino sugar found in calicheamicin, a potent antitumor agent.1,2,3,4,5
Molecular Spectra
No Data Available
Click here to submit data
References
No Data Available
Click here to submit data