Fmoc-S-tert-butyl-L-cysteine structure
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Common Name | Fmoc-S-tert-butyl-L-cysteine | ||
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CAS Number | 67436-13-9 | Molecular Weight | 399.503 | |
Density | 1.2±0.1 g/cm3 | Boiling Point | 603.4±55.0 °C at 760 mmHg | |
Molecular Formula | C22H25NO4S | Melting Point | 135-137ºC | |
MSDS | Chinese USA | Flash Point | 318.7±31.5 °C |
Use of Fmoc-S-tert-butyl-L-cysteineN-(((9H-Fluoren-9-yl)methoxy)carbonyl)-S-(tert-butyl)-L-cysteine is a cysteine derivative[1]. |
Name | Fmoc-Cys(tBu)-OH |
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Synonym | More Synonyms |
Description | N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-S-(tert-butyl)-L-cysteine is a cysteine derivative[1]. |
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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 |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 603.4±55.0 °C at 760 mmHg |
Melting Point | 135-137ºC |
Molecular Formula | C22H25NO4S |
Molecular Weight | 399.503 |
Flash Point | 318.7±31.5 °C |
Exact Mass | 399.150421 |
PSA | 100.93000 |
LogP | 5.84 |
Vapour Pressure | 0.0±1.8 mmHg at 25°C |
Index of Refraction | 1.600 |
Storage condition | 2-8°C |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xi |
Safety Phrases | S22-S24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2930909090 |
~80% Fmoc-S-tert-but... CAS#:67436-13-9 |
Literature: Atherton, Eric; Pinori, Masimo; Sheppard, Robert C. Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1985 , p. 2057 - 2064 |
Precursor 2 | |
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DownStream 0 |
HS Code | 2930909090 |
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Summary | 2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
The investigation of Fmoc-cysteine derivatives in solid phase peptide synthesis.
Pept. Res. 2(1) , 147-52, (1989) Fmoc-Cys(t-Bu)-OH, Fmoc-Cys(Acm)-OH, and Fmoc-Cys(Trt)-OH exhibit excellent synthesis characteristics when used in Fmoc solid phase peptide synthesis on the Applied Biosystems Model 431A peptide synth... |
L-Cysteine, S-(1,1-dimethylethyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]- |
S-tert-Butyl-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-cysteine |
L-Cysteine, S-(1,1-dimethylethyl)-N-((9H-fluoren-9-ylmethoxy)carbonyl)- |
MFCD00037130 |
(2R)-3-tert-butylsulfanyl-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid |
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-S-(2-methyl-2-propanyl)-L-cysteine |
Fmoc-S-t-butyl-cysteine |
Fmoc-S-tert-butyl-L-cysteine |