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Product Name: L-Methionine,N-[(1,1-dimethylethoxy)carbonyl]-, 2,5-dioxo-1-pyrrolidinyl ester
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3845-64-5

3845-64-5 structure

Name: Boc-Met-OSu
Chemical Name: boc-met-osu
CAS Number: 3845-64-5
Molecular Formula: C₁₄H₂₂N₂O₆S
Molecular Weight: 346.399
Catalog: Biochemical Amino acids and their derivatives BOC-amino acid
Create Date: 2016-11-06 10:35:21
Modify Date: 2026-08-07 07:20:28
Boc-Met-OSu is a Methionine (HY-13694) derivative[1].

Name	boc-met-osu
Synonyms	n-hydroxysuccinimidylt-butoxycbonylmethionine 2,5-dioxopyrrolidin-1-yl (2S)-2-{[(tert-butoxy)carbonyl]amino}-4-(methylsulfanyl)butanoate N-Boc-L-methionine N-Succinimidyl Ester Boc-Met-OSu N-(tert-Butoxycbonyl)-L-methionine N-Succinimidyl Ester > N-(tert-Butoxycarbonyl)-L-Methionine N-SucciniMidyl Ester BOC-Met-ONsu 2,5-Dioxo-1-pyrrolidinyl N-{[(2-methyl-2-propanyl)oxy]carbonyl}methioninate N-(tert-Butyloxycbonyl)-L-methionine ester with N-hydroxysuccinimide Boc-L-methionineN-hydroxysuccinimide ester (HPLC) succinimido (S)-2-[(tert-butoxycbonyl)amino]-4-(methylthio)butyrate 1-[(S)-2-[[(1,1-Dimethylethoxy)carbonyl]amino]-4-(methylthio)-1-oxobutoxy]-2,5-pyrrolidinedione BOC-L-METHIONINE HYDROXYSUCCINIMIDE ESTER (2,5-dioxopyrrolidin-1-yl) 2-[(2-methylpropan-2-yl)oxycbonylamino]-4-methylsulfanyl-butanoate (S)-2,5-Dioxopyrrolidin-1-yl2-((tert-butoxycbonyl)amino)-4-(methylthio)butanoate Methionine, N-[(1,1-dimethylethoxy)carbonyl]-, 2,5-dioxo-1-pyrrolidinyl ester N-tert-butyloxycarbonyl-L-methionine N-succinimidoyl ester TBM-NHS Boc-L-Met-OSu Boc-L-methionine hydeoxysuccinimide ester N-(tert-Butoxycbonyl)-L-methionine N-Succinimidyl Ester N-Boc-L-methionine N-Succinimidyl EsterBoc-Met-OSu BOC-MET-OSU //BP BOC-L-METHIONINE HYDROXYSUCCINIMIDESTER tert-butyloxycarbonylmethionine N-hydroxysuccinimide ester (Tert-Butoxy)carbonyl Met-OSu N-ALPHA-T-BOC-L-METHIONINE N-HYDROXYSUCCINIMIDE ESTER BOC-L-METHIONINE N-HYDROXYSUCCINIMIDE ESTER N-Boc-L-methionine N-succinimidyl ester N-alpha-t-Butyloxycbonyl-L-methionine succinimidyl ester N-Boc-L-methionine N-Succinimidyl Ester BOC-METHIONINE-OSU n-hydroxysuccinimidylt-butoxycarbonylmethionine 2-(tert-butoxycbonylamino)-4-(methylthio)butyric acid succinimido ester N-(tert-butoxycbonyl)-L-methionine hydroxysuccinimide L-Methionine, N-[(1,1-dimethylethoxy)carbonyl]-, 2,5-dioxo-1-pyrrolidinyl ester (2,5-dioxopyrrolidin-1-yl) 2-[(2-methylpropan-2-yl)oxycbonylamino]-4-methylsulfanylbutanoate t-Boc-Met-OSu BOC-MET-OSU N-(tert-Butoxycbonyl)methionine 2,5-dioxopyrrolizino TERT-BUTOXYCBONYL-L-METHIONINE N-HYDROXYSUCCINIMIDE ESTER BOC-Met-NHS N-Boc-L-methionine N-hydroxysuccinimide ester

Description	Boc-Met-OSu is a Methionine (HY-13694) 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	120-126ºC
Molecular Formula	C₁₄H₂₂N₂O₆S
Molecular Weight	346.399
Exact Mass	346.119843
PSA	127.31000
LogP	0.63
Appearance	Solid
Index of Refraction	1.536
Storage condition	−20°C

Personal Protective Equipment	Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Safety Phrases	24/25
RIDADR	NONH for all modes of transport
WGK Germany	3
HS Code	29309090

6066-82-6

2488-15-5

~67%

3845-64-5

Literature: Appel, Rolf; Glaesel, Ursula Chemische Berichte, 1980 , vol. 113, # 11 p. 3511 - 3516

2488-15-5

107960-02-1

~91%

3845-64-5

Literature: Jaoudai, Mahmoud; Martinez, Jean; Castro, Bertrand Journal of Organic Chemistry, 1987 , vol. 52, # 12 p. 2364 - 2367

74124-79-1

2488-15-5

~35%

3845-64-5

Literature: Konnert, Laure; Lamaty, Frederic; Martinez, Jean; Colacino, Evelina Journal of Organic Chemistry, 2014 , vol. 79, # 9 p. 4008 - 4017

63-68-3

3845-64-5

Literature: Lyons, Anthony Q.; Pettit, Leslie D. Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999), 1984 , p. 2305 - 2308

Precursor 5
6066-82-6 2488-15-5 107960-02-1 74124-79-1
63-68-3
DownStream 6
23446-03-9 14486-03-4 116939-85-6 18321-99-8
66880-59-9 5920-14-9

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