2697-85-0

2697-85-0 structure

Name: 3β,7β,17β-Trihydroxyandrost-5-ene
Chemical Name: androst-5-en-3b ,7,17b -triol
CAS Number: 2697-85-0
Molecular Formula: C₁₉H₃₀O₃
Molecular Weight: 306.440
Create Date: 2016-01-09 11:56:37
Modify Date: 2024-01-02 15:40:06

Name	androst-5-en-3b ,7,17b -triol
Synonyms	Androst-5-ene-3,7,17-triol, (3β,17β)- Androst-5-ene-3b,7,17b-triol (3β,17β)-Androst-5-ene-3,7,17-triol Androst-5-ene-3beta,7beta,17beta-triol 3β,7β,17β-Trihydroxyandrost-5-ene (3beta,7beta,17beta)-Androst-5-ene-3,7,17-triol

Density	1.2±0.1 g/cm3
Boiling Point	474.3±45.0 °C at 760 mmHg
Melting Point	235-237 ºC
Molecular Formula	C₁₉H₃₀O₃
Molecular Weight	306.440
Flash Point	218.3±23.3 °C
Exact Mass	306.219482
PSA	60.69000
LogP	2.05
Vapour Pressure	0.0±2.7 mmHg at 25°C
Index of Refraction	1.587

521-17-5

~48%

2226-65-5

2697-85-0

Literature: Milecka-Tronina, Natalia; Kolek, Teresa; Swizdor, Alina; Panek, Anna Bioorganic and Medicinal Chemistry, 2014 , vol. 22, # 2 p. 883 - 891

566-19-8

~86%

2697-85-0

Literature: Marwah, Padma; Marwah, Ashok; Lardy, Henry A.; Miyamoto, Hiroshi; Chang, Chawnshang Bioorganic and Medicinal Chemistry, 2006 , vol. 14, # 17 p. 5933 - 5947

53-43-0

~15%

2487-48-1

2697-85-0

Literature: Wang, Yanjie; Sun, Dongmei; Chen, Zhibao; Ruan, Hongsheng; Ge, Wenzhong Biocatalysis and Biotransformation, 2013 , vol. 31, # 4 p. 168 - 174

2099-26-5

2697-85-0

Literature: Butenandt; Hausmann; Paland Chemische Berichte, 1938 , vol. 71, p. 1316,1321

521-17-5

566-19-8

~30%

2226-65-5

2697-85-0

Detail

Literature: Kolek, Teresa; Milecka, Natalia; Swizdor, Alina; Panek, Anna; Bialonska, Agata Organic and Biomolecular Chemistry, 2011 , vol. 9, # 15 p. 5414 - 5422

13209-60-4

555-31-7

67-63-0

2697-85-0

Literature: Schering A.G. Patent: US2170124 , 1936 ; Full Text Show Details Butenandt; Hausmann; Paland Chemische Berichte, 1938 , vol. 71, p. 1316,1321

13209-60-4

2697-85-0

Literature: Schering A.G. Patent: US2170124 , 1936 ; Full Text Show Details Schering-Kahlbaum A.G. Patent: GB486854 , 1936 ; Full Text Show Details Butenandt; Hausmann; Paland Chemische Berichte, 1938 , vol. 71, p. 1316,1321

Precursor 7
521-17-5 566-19-8 53-43-0 13209-60-4
2099-26-5 555-31-7 67-63-0
DownStream 0

2697-85-0	2226-66-6
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