Boc-Met-OSu

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Names

[ CAS No. ]:
3845-64-5

[ Name ]:
Boc-Met-OSu

[Synonym ]:
BOC-L-METHIONINE N-HYDROXYSUCCINIMIDE ESTER
Boc-Met-OSu
N-(tert-Butoxycarbonyl)-L-Methionine N-SucciniMidyl Ester
N-Boc-L-methionine N-Succinimidyl Ester
BOC-Met-ONsu
BOC-METHIONINE-OSU
2,5-Dioxo-1-pyrrolidinyl N-{[(2-methyl-2-propanyl)oxy]carbonyl}methioninate
n-hydroxysuccinimidylt-butoxycarbonylmethionine
BOC-L-METHIONINE HYDROXYSUCCINIMIDE ESTER
Methionine, N-[(1,1-dimethylethoxy)carbonyl]-, 2,5-dioxo-1-pyrrolidinyl ester
t-Boc-Met-OSu
N-tert-butyloxycarbonyl-L-methionine N-succinimidoyl ester
TBM-NHS
Boc-L-Met-OSu
Boc-L-methionine hydeoxysuccinimide ester
N-Boc-L-methionine N-Succinimidyl EsterBoc-Met-OSu
BOC-L-METHIONINE HYDROXYSUCCINIMIDESTER
tert-butyloxycarbonylmethionine N-hydroxysuccinimide ester
N-Boc-L-methionine N-hydroxysuccinimide ester

Chemical & Physical Properties

[ 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 of Characters ]:
Solid

[ Index of Refraction ]:
1.536

[ Storage condition ]:
−20°C

MSDS

Safety Information

[ 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

Synthetic Route

Precursor & DownStream

Precursor

  • N-Hydroxysuccinimide
  • Boc-Met-OH
  • (2,5-dioxopyrrolidin-1-yl) 1,2,2,2-tetrachloroethyl carbonate
  • N,N'-Disuccinimidyl carbonate
  • L-Methionine

DownStream

  • boc-met-gly-oh
  • H-Met-Gly-OH
  • BOC-MET-PRO-OH
  • (2S)-2-[[(2S)-2-formamido-4-methylsulfanylbutanoyl]amino]-4-methylpentanoic acid
  • boc-met-leu-ome
  • N-T-BOC-MET-ASP-PHE AMIDE

Articles

High affinity binding of a glycopeptide elicitor to tomato cells and microsomal membranes and displacement by specific glycan suppressors.

J. Biol. Chem. 268(20) , 14724-31, (1993)

We have previously isolated glycopeptides derived from yeast invertase that acted as highly potent elicitors in suspension-cultured tomato cells, inducing ethylene biosynthesis and phenylalanine ammon...

Peracylation of nucleosides with methionine: foundation for a method to detect carcinogen adducts.

Chem. Res. Toxicol. 7(5) , 650-8, (1994)

We report the chemical foundation for a new method to detect carcinogen-DNA adducts, which we have designated adduct detection by acylation with methionine (ADAM). The method is based on reaction of D...


More Articles


Related Compounds

  • t-Boc-Met-OSu
  • boc-met-gly-osu
  • Boc-D-Met-OSu
  • Boc-Met-β-Ala-Phe-OMe
  • Boc-Met-OH
  • Boc-Met-Leu-OH
  • 2-[(5-Methoxypyridin-2-yl)oxy]propanoic acid
  • 2-((5-Methoxypyrimidin-2-yl)oxy)propanoic acid
  • 2-((1-Isopropyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)oxy)propanoic acid
  • 2-((1-(tert-Butyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)oxy)propanoic acid
  • 2-[(5-Bromopyrimidin-4-yl)oxy]propanoic acid
  • 2-[(6-Methoxyquinolin-2-yl)oxy]acetic acid
  • 2-[(6-Fluoroquinazolin-4-yl)oxy]acetic acid
  • 2-[(2-Cyclopropylpyrimidin-4-yl)oxy]acetic acid
  • 2-{Thieno[3,2-b]pyridin-7-yloxy}acetic acid
  • 2-((3-(Trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)oxy)acetic acid
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