Boc-Met-OSu

Modify Date: 2024-01-17 07:23:44

Boc-Met-OSu Structure
Boc-Met-OSu structure
Common Name Boc-Met-OSu
CAS Number 3845-64-5 Molecular Weight 346.399
Density 1.3±0.1 g/cm3 Boiling Point N/A
Molecular Formula C14H22N2O6S Melting Point 120-126ºC
MSDS Chinese USA Flash Point N/A

 Use of Boc-Met-OSu


Boc-Met-OSu is a Methionine (HY-13694) derivative[1].

 Names

Name boc-met-osu
Synonym More Synonyms

 Boc-Met-OSu Biological Activity

Description Boc-Met-OSu is a Methionine (HY-13694) derivative[1].
Related Catalog
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 1.3±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

 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

~67%

Boc-Met-OSu Structure

Boc-Met-OSu

CAS#:3845-64-5

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

~91%

Boc-Met-OSu Structure

Boc-Met-OSu

CAS#:3845-64-5

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

~35%

Boc-Met-OSu Structure

Boc-Met-OSu

CAS#:3845-64-5

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

~%

Boc-Met-OSu Structure

Boc-Met-OSu

CAS#: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

 Articles2

More 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...

 Synonyms

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
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