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3845-64-5

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3845-64-5 Structure

3845-64-5 Structure
IdentificationBack Directory
[Name]

BOC-MET-OSU
[CAS]

3845-64-5
[Synonyms]

TBM-NHS
BOC-MET-OSU
BOC-Met-NHS
Boc-L-Met-OSu
BOC-METHIONINE-OSU
(Tert-Butoxy)Carbonyl Met-OSu
N-Boc-L-methionine N-succinimidyl ester
BOC-L-METHIONINE HYDROXYSUCCINIMIDESTER
Boc-L-methionine hydeoxysuccinimide ester
BOC-L-METHIONINE HYDROXYSUCCINIMIDE ESTER
BOC-L-METHIONINE N-HYDROXYSUCCINIMIDE ESTER
n-hydroxysuccinimidylt-butoxycarbonylmethionine
N-Boc-L-methionine N-Succinimidyl Ester Boc-Met-OSu
N-ALPHA-T-BOC-L-METHIONINE N-HYDROXYSUCCINIMIDE ESTER
N-(tert-Butoxycarbonyl)methionine 2,5-dioxopyrrolizino
Boc-L-methionineN-hydroxysuccinimide ester≥ 99% (HPLC)
N-(tert-butoxycarbonyl)-L-methionine hydroxysuccinimide
N-(tert-Butoxycarbonyl)-L-methionine N-Succinimidyl Ester
N-alpha-t-Butyloxycarbonyl-L-methionine succinimidyl ester
succinimido (S)-2-[(tert-butoxycarbonyl)amino]-4-(methylthio)butyrate
N-(tert-Butyloxycarbonyl)-L-methionine ester with N-hydroxysuccinimide
2-(tert-butoxycarbonylamino)-4-(methylthio)butyric acid succinimido ester
(S)-2,5-Dioxopyrrolidin-1-yl2-((tert-butoxycarbonyl)amino)-4-(methylthio)butanoate
(2,5-dioxopyrrolidin-1-yl) 2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-methylsulfanylbutanoate
(2,5-dioxopyrrolidin-1-yl) 2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-methylsulfanyl-butanoate
1-[(S)-2-[[(1,1-Dimethylethoxy)carbonyl]amino]-4-(methylthio)-1-oxobutoxy]-2,5-pyrrolidinedione
[EINECS(EC#)]

223-341-9
[Molecular Formula]

C14H22N2O6S
[MDL Number]

MFCD00042760
[MOL File]

3845-64-5.mol
[Molecular Weight]

346.4
Chemical PropertiesBack Directory
[Melting point ]

120-126 °C
[storage temp. ]

−20°C
[form ]

Solid
[color ]

White to Almost white
[Optical Rotation]

[α]20/D 21.5±2°, c = 2% in dioxane
[Sensitive ]

Moisture Sensitive
[BRN ]

4238574
[CAS DataBase Reference]

3845-64-5
Safety DataBack Directory
[Safety Statements ]

24/25
[WGK Germany ]

3
[F ]

3-10-21
[HS Code ]

29309090
Hazard InformationBack Directory
[Uses]

peptide synthesis
[reaction suitability]

reaction type: Boc solid-phase peptide synthesis
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