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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 375613Generated: October 27, 2026

tert-Butyl 2-(methoxy(methyl)amino)-1-methyl-2-oxoethylcarbamate

EOS-60721 · Boc-Ala-N-O · Boc-Ala-NMe(OMe) · Boc-Ala-n(OCH3)CH3 · Boc-L-Ala-N(OCH3)CH3 · BOC-ALA-N(OCH3)CH3 USP/EP/BP · BOC-L-ALANINE N-METHOXY-N-METHYL AMIDE · Boc-L-alanine-N'-methoxy-N'-carboxamide

https://huagongshe.com/en/chemical/375613

tert-Butyl 2-(methoxy(methyl)amino)-1-methyl-2-oxoethylcarbamate molecular structure

Identifiers & Physical Properties

CAS No.87694-49-3
Molecular formulaC10H20N2O4
Average molar mass232.28 g/mol
Monoisotopic mass232.14230712 g/mol
SMILESCON(C)C(=O)C(C)NC(=O)OC(C)(C)C
InChIKeyPWQIGBOSLQHOBT-UHFFFAOYSA-N
PubChem CID375613

Chemical & Physical Properties

XLogP0.9
Topological polar surface area67.9
Hydrogen bond donors1
Hydrogen bond acceptors4
Rotatable bonds5
Heavy atoms16
Formal charge0
Complexity260
Melting point148-153 °C (lit.)
Density1.070
Storage conditionsKeep in dark place,Sealed in dry,Room Temperature
Solubilitysoluble in Methanol
pKa (acidity coefficient)11.19±0.46(Predicted)
Physical stateCrystalline Powder or Powder
ColorWhite to off-white
optical activity[α]24/D 26°, c = 1 in methanol
Major applicationspeptide synthesis
InChIInChI=1/C10H20N2O4/c1-7(8(13)12(5)15-6)11-9(14)16-10(2,3)4/h7H,1-6H3,(H,11,14)/t7-/s3
InChIKeyPWQIGBOSLQHOBT-ZETCQYMHSA-N
SMILESC(OC(C)(C)C)(=O)N[C@@H](C)C(N(OC)C)=O |&1:8,r|
UNSPSC Code12352200
NACRESNA.22
GHS pictogramGHS07
Signal wordWarning
GHS hazard statementsH302-H315-H319-H335
GHS precautionary statementsP261-P301+P312-P302+P352-P304+P340-P305+P351+P338
Water hazard class (WGK)3
Customs code2924297099
Storage class11 - Combustible Solids

Safety & Regulations

Water hazard class (WGK)3
Customs code2924297099
Signal wordWarning
GHS pictogramGHS07
Storage class11 - Combustible Solids
GHS hazard statementsH302-H315-H319-H335
GHS precautionary statementsP261-P301+P312-P302+P352-P304+P340-P305+P351+P338

Applications & Uses

Uses

Reduced by LiAlH4 to give the corresponding Boc-amino acid aldehyde.

Uses

α-Amino Weinreb amide.