TERT-BUTYL (S)-(-)-4-FORMYL-2,2-DIMETHYL-3-OXAZOLIDINECARBOXYLATE

Name	tert-butyl (S)-(-)-4-formyl-2,2-dimethyl-3-oxazol
Synonyms	(S)-Garner aldehyde Butoxycarbonylformyldimethyloxazolidine (S)-3-BOC-4-FORMYL-2,2-DIMETHYL-1,3-OXAZOLIDINE )-3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde tert-butyl (S)-(-)-4-formyl-2,2-dimethyl-3-oxazol (S)-(-)-3-BOC-4-FORMYL-2,2-DIMETHYL-1,3-OXAZOLIDINE (S)-()-3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde TERT-BUTYL (S)-(-)-4-FORMYL-2,2-DIMETHYL-3-OXAZOLIDINECARBOXYLATE tert-butyl (4S)-4-formyl-2,2-dimethyl-1,3-oxazolidine-3-carboxylate (S)-(-)-3-TERT-BUTOXYCARBONYL-4-FORMYL-2,2-DIMETHYL-1,3-OXAZOLIDINE (S)-(-)-3-tert-Butoxycarbonyl-4-formyl-2,2-dimethyl-1,3-oxazolidine 1,1-DIMETHYLETHYL-(S)-4-FORMYL-2,2-DIMETHYL-3-OXAZOLIDINE CARBOXYLATE (S)-4-FORMYL-2,2-DIMETHYL-OXAZOLIDINE-3-CARBOXYLIC ACID TERT-BUTYL ESTER (4S)-3-(tert-Butoxycarbonyl)-2,2-dimethyl-1,3-oxazolidine-4-carbaldehyde
CAS	102308-32-7
InChI	InChI=1/C11H19NO4/c1-10(2,3)16-9(14)12-8(6-13)7-15-11(12,4)5/h6,8H,7H2,1-5H3/t8-/m1/s1

Molecular Formula	C11H19NO4
Molar Mass	229.27
Density	1.06g/mLat 25°C(lit.)
Boling Point	83-88°C1mm Hg(lit.)
Specific Rotation(α)	D -91.7° (c = 1.34 in CHCl3)
Flash Point	226°F
Water Solubility	Slightly soluble in water.
Solubility	Chloroform (Slightly), Methanol (Slightly)
Vapor Presure	0.001mmHg at 25°C
Appearance	Transparent colorless to yellow oily
Color	Clear colorless to yellow
BRN	3591324
pKa	-3.26±0.60(Predicted)
Storage Condition	Inert atmosphere,2-8°C
Sensitive	Air Sensitive
Refractive Index	n20/D 1.445(lit.)
MDL	MFCD00209557
Use	This product is for scientific research only and shall not be used for other purposes.

Hazard Symbols	Xi - Irritant
Risk Codes	36/37/38 - Irritating to eyes, respiratory system and skin.
Safety Description	S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. S37/39 - Wear suitable gloves and eye/face protection
WGK Germany	3
HS Code	29349990

Introduction	3-trans-bromocarbon -2,2 '-dimethyloxate is transparent colorless to yellow oil and can be used as an intermediate in organic synthesis for organic experimental synthesis.
Synthesis method	Using L-serine as the starting material, Garner aldehyde is prepared by Boc protection, namely 3-trans-bromocarbon -2,2 '-Dimethyloxate. The synthesis reaction formula of 3-trans-bromocarbon -2,2 '-dimethyloxylate is as follows:
use	is widely used in asymmetric synthesis of natural products.

Last Update：2024-04-09 21:11:58

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TERT-BUTYL (S)-(-)-4-FORMYL-2,2-DIMETHYL-3-OXAZOLIDINECARBOXYLATE Request for Quotation