CAS No.149794-10-5,BOC-N-ETHYL GLYCINE Suppliers

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Basic Information

Molecular Structure:
CAS No.:	149794-10-5
Name:	BOC-N-ETHYL GLYCINE
Article Data:	18

Formula:	C₉H₁₇NO₄
Molecular Weight:	203.238
Synonyms:	N-(tert-Butoxycarbonyl)-N-ethylaminoacetic acid;N-Boc-N-ethylglycine;N-tert-Butoxycarbonyl-N-ethylglycine;2-(N-Ethyl-N-tert-butoxycarbonylamino)aceticacid;
Density:	1.114 g/cm³
Melting Point:	87-88℃
Boiling Point:	302.729 °C at 760 mmHg
Flash Point:	136.886 °C
Hazard Symbols:	Xn
Risk Codes:	22
PSA:	66.84000
LogP:	1.32800

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Specification

The Glycine, N-[(1, 1-dimethylethoxy)carbonyl]-N-ethyl-, with the CAS registry number 149794-10-5, is also known as N-(tert-Butoxycarbonyl)-N-ethylglycine. It belongs to the product categories of Amino Acid Derivatives; Amino Acids. This chemical's molecular formula is C₉H₁₇NO₄ and molecular weight is 203.24. What's more, its IUPAC name is 2-[Ethyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]acetic acid. In addition, it must be stored at 0 °C.

Physical properties about Glycine, N-[(1, 1-dimethylethoxy)carbonyl]-N-ethyl- are: (1)ACD/LogP: 1.75; (2)# of Rule of 5 Violations: 0; (3)ACD/BCF (pH 5.5): 1; (4)ACD/BCF (pH 7.4): 1; (5)ACD/KOC (pH 5.5): 3; (6)ACD/KOC (pH 7.4): 1; (7)#H bond acceptors: 5; (8)#H bond donors: 1; (9)#Freely Rotating Bonds: 5; (10)Polar Surface Area: 66.84 Å²; (11)Index of Refraction: 1.468; (12)Molar Refractivity: 50.771 cm³; (13)Molar Volume: 182.506 cm³; (14)Polarizability: 20.127×10^-24 cm³; (15)Surface Tension: 39.496 dyne/cm; (16)Density: 1.114 g/cm³; (17)Flash Point: 136.886 °C; (18)Enthalpy of Vaporization: 59.721 kJ/mol; (19)Boiling Point: 302.729 °C at 760 mmHg; (20)Vapour Pressure: 0 mmHg at 25 °C.

Uses of Glycine, N-[(1, 1-dimethylethoxy)carbonyl]-N-ethyl-: it is used to produce other chemicals. For example, it is used to produce N-(tert-Butoxycarbonyl)-N-ethylglycine methylamide. This reaction needs reagents N-Hydroxysuccinimide, Dicyclohexylcarbodiimide, Triethylamine. Meanwhile, it needs solvent Dimethylformamide. The reaction time is 24 hours. The yield is about 46 %.

Glycine, N-[(1, 1-dimethylethoxy)carbonyl]-N-ethyl- can react with Methylamine; hydrochloride to get N-(tert-Butoxycarbonyl)-N-ethylglycine methylamide.

You can still convert the following datas into molecular structure:
(1) SMILES: CC(C)(C)OC(=O)N(CC)CC(O)=O
(2) InChI: InChI=1/C9H17NO4/c1-5-10(6-7(11)12)8(13)14-9(2,3)4/h5-6H2,1-4H3,(H,11,12)
(3) InChIKey: SPBIXXXFDSLALC-UHFFFAOYAS