145164-84-7

Basic information

• Product Name: estradiol
• Synonyms: estradiol
• CAS NO: 145164-84-7
• Molecular Weight: 272.387
• Mol File: 145164-84-7.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: estradiol(CAS DataBase Reference)
• NIST Chemistry Reference: estradiol(145164-84-7)
• EPA Substance Registry System: estradiol(145164-84-7)

Safety Data

• Hazardous Substances Data: 145164-84-7(Hazardous Substances Data)

Upstream product

• 100-84-5 1-methoxy-3-methyl-benzene 
• 27060-75-9 4-bromo-3-methylanisole 
• 52289-54-0 4-methoxysalicylaldehyde 
• 75863-04-6 rac-3-Methoxy-6,7:8,9-diseco-1,3,5⁽¹⁰⁾,7-oestratetraen-9,17-dion 
• 19973-76-3 (+/-)-oestrone 
• 1239-35-6 16α-bromo-3-hydroxy-1,3,5(10)-estratrien-17-one 3-acetate 
• 75863-25-1 2-Trimethylsilyl-1-(4-methoxy-2-methylphenyl)prop-2-en-1-on 
• 75863-24-0 (1Ξ,5SR)-1-Methyl-2-oxo-5-vinylcyclopentan-1,3-dicarbonsaeure-dimethylester 
• 80868-65-1 2-Trimethylsilyl-1-(4-methoxy-2-methylphenyl)prop-2-en-1-ol 
• 75863-10-4 <(6Ξ,7SR)-6-Methyl-1,4-dioxaspiro<4.4>non-7-yl>essigsaeure-methylester 
• 75863-12-6 (6Ξ,7SR)-6-Methyl-7-vinyl-1,4-dioxaspiro<4.4>nonan 
• 75863-11-5 2-<(6Ξ,4SR)-6-Methyl-1,4-dioxaspiro<4.4>non-7-yl>ethanol 
• 80868-64-0 1-(4-Methoxy-2-methylphenyl)prop-2-en-1-ol 
• 80868-66-2 1-(4-Methoxy-2-methylphenyl)prop-2-en-1-on 

Downstream Products

• 1474-52-8 17β-oestradiol diacetate 
• 1743-60-8 17-β-estradiol 17-acetate 
• 24381-12-2 2-iodo-17β-oestradiol 
• 15833-07-5 2-bromo-17β-oestradiol 
• 88847-87-4 2-chloro-17β-oestradiol 
• 53-16-7 Estrone 
• 1624-62-0 estrone 3-methyl ether 
• 1035-77-4 estradiol 3-methyl ether, 17-ol 

Relevant articles and documents

A Total Synthesis of Estradiol and its 6,6-Dimethyl Analogue

A short, stereoselective synthesis of estradiol, and its 6,6-dimethyl analogue, was accomplished from non-steroidal starting materials.A key feature was the use of a benzothiophene unit to effect (i) the stereoselective formation of the required 8β-H c

Syntheses of Seleno Estrogens

The syntheses of phenylseleno and methylseleno analogues of estradiol are described.

Asymmetric total synthesis of estradiol by an intramolecular cycloaddition of benzocyclobutene derivative

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