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35418-16-7

tert-butyl 5-oxo-L-prolinate

CAS: 35418-16-7

Molecular Formula: C9H15NO3

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35418-16-7 - Names and Identifiers

Name tert-butyl 5-oxo-L-prolinate
Synonyms L-Pyr-Otbu
H-Pyr-OtBu
tert-Butyl L-PyroglutaMate
tert-butyl 5-oxo-L-prolinate
tert-Butyl 5-oxo-L-prolinate
L-PyroglutaMic acid ter-butyl ester
2-Methyl-2-propanyl 5-oxo-L-prolinate
L-Proline,5-oxo-, 1,1-diMethylethyl ester
tert-Butyl (S)-5-oxo-2-pyrrolidinecarboxylate
(S)-tert-Butyl 5-oxopyrrolidine-2-carboxylate
tert-butyl (2S)-5-oxopyrrolidine-2-carboxylate
CAS 35418-16-7
EINECS 252-555-5
InChI InChI=1/C9H15NO3/c1-9(2,3)13-8(12)6-4-5-7(11)10-6/h6H,4-5H2,1-3H3,(H,10,11)/t6-/m0/s1

35418-16-7 - Physico-chemical Properties

Molecular FormulaC9H15NO3
Molar Mass185.22
Density1.099±0.06 g/cm3(Predicted)
Melting Point102.0 to 108.0 °C
Boling Point319.2±35.0 °C(Predicted)
Flash Point146.8°C
Vapor Presure0.000344mmHg at 25°C
AppearanceWhite solid
ColorWhite
BRN3590226
pKa14.65±0.40(Predicted)
Storage ConditionSealed in dry,Room Temperature
Refractive Index1.467
MDLMFCD06659481

35418-16-7 - Risk and Safety

Hazard SymbolsXi - Irritant
Irritant
Risk Codes36/38 - Irritating to eyes and skin.
Safety Description26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
WGK Germany3
HS Code29339900

35418-16-7 - Introduction

tert-butyl 5-oxo-L-prolinate(tert-butyl 5-oxo-L-prolinate) is an organic compound whose chemical formula is C9H15NO3.

Nature:
tert-butyl 5-oxo-L-prolinate is a white crystalline solid that is stable at ambient temperatures. Its solubility is relatively low, soluble in some organic solvents such as ethanol and dimethylformamide.

Use:
tert-butyl 5-oxo-L-prolinate is commonly used as an optically active substance, and is often used as a substrate or ligand for chiral catalytic reactions in organic synthesis. It has good chemical stability and excellent stereoselectivity, and is widely used in pharmaceutical, material science and pesticide fields.

Preparation Method:
tert-butyl 5-oxo-L-prolinate has a variety of preparation methods, and the common method is to synthesize by job isotope exchange or acetic anhydride method. First, the intermediate of tert-butyl pyroglutamate is obtained by reacting pyroglutamic acid with tert-butoxyl chloride, which is converted to the tert-butyl 5-oxo-L-prolinate by an appropriate method.

Safety Information:
tert-butyl 5-oxo-L-prolinate has low toxicity, laboratory safety procedures still need to be followed. Avoid contact with skin and eyes. Wear protective gloves and safety glasses if necessary. Avoid producing dust or gas during operation or storage. Seek immediate medical assistance if exposed or inhaled.
Last Update:2024-04-10 22:29:15
35418-16-7
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