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13798-75-9

13798-75-9 structure

13798-75-9 structure

Name: Boc-Asp(OBzl)-OSu
Chemical Name: (S)-4-Benzyl 1-(2,5-dioxopyrrolidin-1-yl) 2-((tert-butoxycarbonyl)amino)succinate
CAS Number: 13798-75-9
Molecular Formula: C₂₀H₂₄N₂O₈
Molecular Weight: 420.413
Catalog: Research Areas Others
Create Date: 2018-12-17 18:31:03
Modify Date: 2026-07-07 16:08:51
Boc-Asp(OBzl)-OSu is an aspartic acid derivative[1].

Name	(S)-4-Benzyl 1-(2,5-dioxopyrrolidin-1-yl) 2-((tert-butoxycarbonyl)amino)succinate
Synonyms	BOC-L-ASPTIC ACID-BETA-BENZYL-ALPHA-HYDROXYSUCCINIMIDE ESTER boc-l-asptic acid 4-benzyl 1-(n-hydroxysuccinimide) Boc-L-aspartic acid 4-benzyl 1-(hydroxysuccinimide) ester Boc-L-asptic acid 4-benzyl 1-(N-hydroxysuccinimide) ester Boc-L-Asp(OBzl)-OSu N-alpha-t-Butyloxycbonyl-L-asptic acid alpha-succinimidyl beta-benzyl ester 2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]butanedioic acid O1-(2,5-dioxo-1-pyrrolidinyl) ester O4-(phenylmethyl) ester Boc-L-Asp(Bzl)-OSu BOC-ASP(OBZL)-OSU N-ALPHA-T-BOC-L-ASPTIC ACID BETA-BENZYL ESTER N-HYDROXYSUCCINIMIDE ESTER 1-benzyl 2,5-dioxopyrrolidin-1-yl (3S)-3-{[(tert-butoxy)carbonyl]amino}butanedioate (Tert-Butoxy)carbonyl Asp(OBzl)-OSu BOC-ASPTIC ACID(OBZL)-OSU BOC-L-ASPTIC ACID-B-BENZYL-A-HYDROXYSUCCINIMIDESTER Boc-Asp(OBzl)-OSu Boc-L-asptic acid α-N-hydroxysucciniMide ester L-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-(2,5-dioxo-1-pyrrolidinyl) 4-(phenylmethyl) ester (S)-4-benzyl 1-(2,5-dioxopyrrolidin-1-yl) 2-(tert-butoxycbonylamino)succinate BOC-L-ASPTIC ACID BETA-BENSYL ESTER N-HYDROXYSUCCINIMIDE ESTER N-tert-Butoxycbonyl-L-asptic acid benzyl-1-(N-hydroxysuccinimide)ester L-Asptic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-(2,5-dioxo-1-pyrrolidinyl) 4-(phenylmethyl) ester Boc-L-Asptic acid β-benzyl α-N-hydroxysuccinim 4-Benzyl 1-(2,5-dioxo-1-pyrrolidinyl) N-{[(2-methyl-2-propanyl)oxy]carbonyl}-L-aspartate Boc-L-asptic acid β-benzyl ester N-hydroxysuccinimide ester Boc-Asp(ObBzl)-OSu BOC-L-ASPTIC ACID BETA-BENZYL-ALPHA-N-HYDROXYSUCCINIMIDE DI-ESTER N-t-BOC-L-aspticacid-benzylester-hydroxysuccinimid REF DUPL: Boc-Asp(OBzl)-OSu 4-Benzyl 1-(2,5-dioxopyrrolidin-1-yl) (tert-butoxycbonyl)-L-asptate N-[(1,1-DIMETHYLETHOXY)carbonyl]-1-(2,5-DIOXO-1-PYRROLIDINYL)-L-ASPTIC ACID 4-(PHENYLMETHYL) ESTER Boc-L-Asptic acid β-benzyl α-N-hydroxysuccinimide ester BOC-L-ASPTIC ACID 4-BENZYL 1-(HYDROXYSUCCINIMIDE) ESTER BOC-L-ASPTIC ACID BETA-BENZYL-HYDROXYSUCCINIMIDE ESTER 4-O-benzyl 1-O-(2,5-dioxopyrrolidin-1-yl) (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanedioate Boc-L-asptic acid α-N-hydroxysuccinimide ester Boc-L-asptic acid β-benzyl esterN-hydroxysuccinimide ester (HPLC) NALPHA-tert-Butoxycbonyl-L-asptic acid B-benzyl 1-(N-hydroxysuccinimide

Description	Boc-Asp(OBzl)-OSu 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.

Density	1.3±0.1 g/cm3
Melting Point	98-102ºC
Molecular Formula	C₂₀H₂₄N₂O₈
Molecular Weight	420.413
Exact Mass	420.153259
PSA	128.31000
LogP	1.92
Index of Refraction	1.560

Personal Protective Equipment	Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADR	NONH for all modes of transport

6066-82-6 structure

6066-82-6

7536-58-5 structure

7536-58-5

~74%

13798-75-9 structure

13798-75-9

Literature: Harris, Thomas D.; Rajopadhye, Milind; Damphousse, Paul R.; Glowacka, Danuta; Yu, Karmine; Bourque, Jeffrey P.; Barrett, John A.; Damphousse, David J.; Heminway, Stuart J.; Lazewatsky, Joel; Mazaika, Theresa; Carroll, Timothy R. Bioorganic and Medicinal Chemistry Letters, 1996 , vol. 6, # 15 p. 1741 - 1746

Precursor 2
6066-82-6 7536-58-5
DownStream 1
35309-53-6

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