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4-pregnene-17α,20β,21-triol-3,11-dione is a complex steroid molecule derived from the pregnane family, characterized by its unique structure and functional groups. 4-pregnene-17 alpha,20 beta,21-triol-3,11-dione features a pregnane core, with three hydroxyl groups at the 17α, 20β, and 21 positions, and two ketone groups at the 3 and 11 positions. It plays a significant role in various biological processes, particularly in the synthesis of hormones such as cortisol and aldosterone, which are crucial for regulating metabolism, immune response, and electrolyte balance. Due to its structural complexity and potential applications in pharmaceuticals, this chemical has been a subject of interest for researchers in the field of endocrinology and drug development.

3615-87-0

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3615-87-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3615-87-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,1 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3615-87:
(6*3)+(5*6)+(4*1)+(3*5)+(2*8)+(1*7)=90
90 % 10 = 0
So 3615-87-0 is a valid CAS Registry Number.
InChI:InChI=1/C21H30O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h9,14-15,17-18,22,25-26H,3-8,10-11H2,1-2H3/t14-,15-,17-,18+,19-,20-,21-/m0/s1

3615-87-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 17α,20S,21-trihydroxypregn-4-ene-3,11-dione

1.2 Other means of identification

Product number -
Other names 17α,20,21-trihydroxypregn-4-ene-3,11-dione

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3615-87-0 SDS

3615-87-0Upstream product

3615-87-0Downstream Products

3615-87-0Relevant academic research and scientific papers

Steroid transformations with Fusarium oxysporum var. cubense and Colletotrichum musae

Wilson, Maureen R.,Gallimore, Winklet A.,Reese, Paul B.

, p. 834 - 843 (2007/10/03)

The utility of two locally isolated fungi, pathogenic to banana, for steroid biotransformation has been studied. The deuteromycetes Fusarium oxysporum var. cubense (IMI 326069, UAMH 9013) and Colletotrichum musae (IMI 374528, UAMH 8929) had not been examined previously for this potential. In general, F. oxysporum var. cubense effected 7α hydroxylation on 3β-hydroxy- Δ5-steroids, 6β, 12β, and 15α hydroxylation on steroidal-4-ene-3-ones, side-chain degradation on 17α,21-dihydroxypregnene-3,20-diones, and 15α hydroxylation on estrone. Both strains were shown to perform redox reactions on alcohols and ketones.

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