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7535-56-0

7535-56-0 structure
7535-56-0 structure
  • Name: Boc-Phe-ONP
  • Chemical Name: (4-nitrophenyl) (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoate
  • CAS Number: 7535-56-0
  • Molecular Formula: C20H22N2O6
  • Molecular Weight: 386.39800
  • Catalog: Biochemical Amino acids and their derivatives BOC-amino acid
  • Create Date: 2018-05-25 08:00:00
  • Modify Date: 2024-01-10 19:29:38
  • 4-Nitrophenyl (tert-butoxycarbonyl)-L-phenylalaninate is a phenylalanine derivative[1].
Name (4-nitrophenyl) (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoate
Synonyms tert-butoxycarbonyl-L-phenylalanine p-nitrophenyl ester
EINECS 231-404-7
N-tert-butoxycarbonyl L-phenylalanine p-nitrophenyl ester
Boc-Phe-ONp
N-tert-butyloxycarbonyl-L-phenylalanine p-nitrophenyl ester
4-NITROPHENYL N-TERT-BUTYLOXYCARBONYL-L-PHENYLALANINATE
MFCD00042811
N-tert-butyloxycarbonyl-L-phenylalanine 4-nitrophenyl ester
AmbotzBAA5870
Boc-L-phenylalanine 4-nitrophenyl ester
N-t-butoxycarbonyl-L-phenylalanine 4-nitrophenyl ester
Description 4-Nitrophenyl (tert-butoxycarbonyl)-L-phenylalaninate is a phenylalanine 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):1793-855.
Density 1.24g/cm3
Boiling Point 558.4ºC at 760mmHg
Melting Point 127-128ºC
Molecular Formula C20H22N2O6
Molecular Weight 386.39800
Flash Point 291.5ºC
Exact Mass 386.14800
PSA 110.45000
LogP 4.55030
Index of Refraction 1.567
Storage condition −20°C
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADR NONH for all modes of transport
WGK Germany 3
100-02-7 structure

100-02-7

13734-34-4 structure

13734-34-4

~81%

7535-56-0 structure

7535-56-0

Literature: Vapirov; Tunina Russian Journal of General Chemistry, 1997 , vol. 67, # 7 p. 1092 - 1094
13734-34-4 structure

13734-34-4

107960-06-5 structure

107960-06-5

~62%

7535-56-0 structure

7535-56-0

Literature: Jaoudai, Mahmoud; Martinez, Jean; Castro, Bertrand Journal of Organic Chemistry, 1987 , vol. 52, # 12 p. 2364 - 2367
100-02-7 structure

100-02-7

~%

7535-56-0 structure

7535-56-0

Literature: Journal of Organic Chemistry, , vol. 52, # 12 p. 2364 - 2367
1070-19-5 structure

1070-19-5

~%

7535-56-0 structure

7535-56-0

Literature: Chemische Berichte, , vol. 97, p. 1819 - 1828
2577-90-4 structure

2577-90-4

~%

7535-56-0 structure

7535-56-0

Literature: Chemische Berichte, , vol. 97, p. 1819 - 1828
16214-37-2 structure

16214-37-2

75-65-0 structure

75-65-0

~%

7535-56-0 structure

7535-56-0

Literature: Chemische Berichte, , vol. 100, p. 3314 - 3318
13303-10-1 structure

13303-10-1

16480-57-2 structure

16480-57-2

~%

7535-56-0 structure

7535-56-0

Literature: Journal of the Chemical Society [Section] C: Organic, , p. 689 - 690

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title: CAS No. 7535-56-0 | Chemsrc address: https://www.chemsrc.com/en/baike/406875.html

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