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5740-62-5

5740-62-5

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5740-62-5 Usage

Uses

Prednisolone 21-Propionate is a derivative of Prednisolone (P703740), synthetic corticosteroid; metabolically interconvertible with prednisone. Prednicarbate USP Related Compound C.

Check Digit Verification of cas no

The CAS Registry Mumber 5740-62-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,4 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5740-62:
(6*5)+(5*7)+(4*4)+(3*0)+(2*6)+(1*2)=95
95 % 10 = 5
So 5740-62-5 is a valid CAS Registry Number.

5740-62-5 Well-known Company Product Price

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  • USP

  • (1554931)  Prednicarbate Related Compound C  United States Pharmacopeia (USP) Reference Standard

  • 5740-62-5

  • 1554931-20MG

  • 14,578.20CNY

  • Detail

5740-62-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-[(8S,9S,10R,11S,13S,14S,17R)-11,17-dihydroxy-10,13-dimethyl-3-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-yl]-2-oxoethyl] propanoate

1.2 Other means of identification

Product number -
Other names Pregna-1,4-diene-3,20-dione,11,17-dihydroxy-21-(1-oxopropoxy)-,(11beta)

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:5740-62-5 SDS

5740-62-5Downstream Products

5740-62-5Relevant articles and documents

Investigation on the Photostability of Halometasone and Prednicarbate in the Crystal State and Crystal Structure of Halometasone

Reisch, Johannes,Henkel, Gerald,Ekiz-Guecer, Nurten,Nolte, Gerald

, p. 63 - 68 (2007/10/02)

UV irradiation of halometasone (1) in the crystal state yields three photoproducts: 2-chloro-6α,9-difluoro-11β,17α-dihydroxy-16-α-methyl-3-oxoandrosta-1,4-diene-17β-carbaldehyde (3), 2-chloro-6α,9-difluoro-11β-hydroxy-16α-methylandrosta-1,4-diene-3,17-dione (4) and the dimerization product 2ξ-chloro-2ξ-(2-chloro-6α,9-difluoro-11β,21ξ-trihydroxy-16α-methyl-3,20-dioxopregna-1,4-dien-21-yl)-6α,9-difluoro-11β,17,21-trihydroxy-16α-methylpregna-4-ene-3,20-dione (5).The structure of 5 is determined by the molecular packing of 1 in the crystal, as shown by an X-ray analysis of 1.Two photoproducts are formed after irradiation of prednicarbate (2): 11β,17-dihydroxy-21-propionyloxypregna-1,4-diene-3,20-dione (6) and 17-(ethoxycarbonyloxy)-11β,21-dihydroxypregna-1,4-diene-3,20-dione (7). Key Words: Prednicarbate / Halometasone / Photochemistry

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