Substance
ID:331278
Names and Identifiers
IUPAC name
(2S)-4-(benzyloxy)-2-{[(tert-butoxy)carbonyl]amino}-4-oxobutanoic acid
IUPAC Traditional name
(2S)-4-(benzyloxy)-2-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid
Synonyms
Boc-Asp(OBzl)-OHBoc-L-aspartic acid 4-benzyl esterBoc-L-天冬氨酸-4-苄酯N-(tert-Butoxycarbonyl)-L-aspartic acid 4-benzyl esterN-(叔丁氧羰基)-L-天冬氨酸-4-苄酯
Registration numbers
CAS Number
Beilstein Number
PubChem SID
MDL Number
EC Number
Properties
Safety Information
MSDS Link
German water hazard class
3
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Product Information
Purity
98%
Linear Formula
C6H5CH2OCOCH2CH(COOH)NHCOOC(CH3)3
Physical Property
Optical Rotation
[α]20/D -19.5°, c = 2 in DMF
Melting Point
98-102 °C(lit.)
Molecule Details
Application
Starting material for the enantiospecific synthesis of (R)-(+)-Boc-iturinic acid (n-C14),1 the L-aspartic series of thrombin inhibitors,2 and diketopiperazine tetrapeptides.3 Used in the preparation of a novel tricyclic dipeptide mimetic based on a [6H]-azepino indoline nucleus.4
Packaging
25 g in glass bottle
Starting material for the enantiospecific synthesis of (R)-(+)-Boc-iturinic acid (n-C14),1 the L-aspartic series of thrombin inhibitors,2 and diketopiperazine tetrapeptides.3 Used in the preparation of a novel tricyclic dipeptide mimetic based on a [6H]-azepino indoline nucleus.4
Packaging
25 g in glass bottle
Molecular Spectra
No Data Available
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References
No Data Available
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