Boc-Asp(OBzl)-OH structure, CAS 7536-58-5

Boc-Asp(OBzl)-OH

CAS Number7536-58-5

Synonyms(2S)-4-(benzyloxy)-2-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid (non-preferred name); EINECS 231-406-8; N-tert-Butoxycarbonyl-L-aspartic acid 4-benzyl ester; MFCD00065564; (2S)-4-(Benzyloxy)-2-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-4-oxobutanoic acid; (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxo-4-phenylmethoxybutanoic acid; L-Aspartic acid, N-((1,1-dimethylethoxy)carbonyl)-, 4-(phenylmethyl) ester; L-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 4-(phenylmethyl) ester; N-α-t-BOC-L-aspartic-β-benzyl ester; Boc-Asp(OBzl)-OH; Boc-L-asparticacid4-benzylester

Molecular FormulaC16H21NO6

Molecular Weight323.34

Purity≥98 (TLC)%

Density1.2±0.1 g/cm3

Boiling Point508.1±50.0 °C at 760 mmHg

Melting Point98-102ºC

Flash Point

Appearancepowder

EINECS231-406-8

MSDSChineseEnglish

Symbol

Signal Word

Cat. No.: 2A-9007265 Purity: ≥98 (TLC)%
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Quality Control of [ 7536-58-5 ] Purity: ≥98 (TLC)% SDS Specification MoL

Chemical & Physical Properties
CAS Number7536-58-5
Catalog No.2A-9007265
Chinese NameBoc-L-天冬氨酸 4-苄酯
Synonyms(2S)-4-(benzyloxy)-2-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid (non-preferred name); EINECS 231-406-8; N-tert-Butoxycarbonyl-L-aspartic acid 4-benzyl ester; MFCD00065564; (2S)-4-(Benzyloxy)-2-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-4-oxobutanoic acid; (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxo-4-phenylmethoxybutanoic acid; L-Aspartic acid, N-((1,1-dimethylethoxy)carbonyl)-, 4-(phenylmethyl) ester; L-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 4-(phenylmethyl) ester; N-α-t-BOC-L-aspartic-β-benzyl ester; Boc-Asp(OBzl)-OH; Boc-L-asparticacid4-benzylester
Molecular FormulaC16H21NO6
Molecular Weight323.34
Purity≥98 (TLC)
Density1.2±0.1 g/cm3
Boiling Point508.1±50.0 °C at 760 mmHg
Melting Point98-102ºC
Appearancepowder
Storage ConditionThis product should be sealed and stored in a dry
Application(2S)-4-(phenoxy)-2-[(tert-butoxycarbonyl)amino]-4-oxobutyric acid is an aspartic acid derivative [1].
EINECS231-406-8
HTC2924299090
MDL NumberMFCD00065564
SMILESN(C(CC(=O)OCc1ccccc1)C(=O)O)C(=O)OC(C)(C)C
InChI1S/C16H21NO6/c1-16(2,3)23-15(21)17-12(14(19)20)9-13(18)22-10-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,17,21)(H,19,20)
InChI KeySOHLZANWVLCPHK-UHFFFAOYSA-N
NACRES CodeNA.22
eCl@ss32160406
UNSPSC12352209
Safety DescriptionS22;S24/25
MSDSmsds/7265_1_7536_58_5.pdf
Bioactivity(2S)-4-(Benzyloxy)-2-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid is an aspartic acid derivative[1]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1]. References [1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144. Chemical & Physical Properties Density 1.2±0.1 g/cm3 Boiling Point 508.1±50.0 °C at 760 mmHg Melting Point 98-102ºC Molecular Formula C16H21NO6 Molecular Weight 323.341 Flash Point 261.1±30.1 °C Exact Mass 323.136902 PSA 101.93000 LogP 3.24 Vapour Pressure 0.0±1.4 mmHg at 25°C Index of Refraction 1.527 InChIKey SOHLZANWVLCPHK-UHFFFAOYSA-N SMILES CC(C)(C)OC(=O)NC(CC(=O)OCc1ccccc1)C(=O)O
Use of(2S)-4-(Benzyloxy)-2-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid is an aspartic acid derivative[1]. Properties Name Boc-L-Asp(OBzl)-OH Synonym More Synonyms Boc-L-aspartic acid 4-benzyl ester Biological Activity Description (2S)-4-(Benzyloxy)-2-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid is an aspartic acid derivative[1]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1]. References [1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144. Chemical & Physical Properties Molecular Formula C16H21NO6 Exact Mass 323.136902 PSA 101.93000 Index of Refraction 1.527 InChIKey SOHLZANWVLCPHK-UHFFFAOYSA-N
Tax Rebate13.0%
SupervisionNone. MFN tariff: 6.5%. Ordinary tariff: 30.0%
Transport InfoProduct name: Purity: 98.0%
MSDS Transport InfoModule 14. Shipping information United Nations classification: inconsistent with United Nations classification standards UN number: not specified
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