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6677-98-1

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6677-98-1 Usage

Uses

Hydrocortisone 21-Propionate is a metabolite of Hydrocortisone 17-Butyrate 21-Propionate (H714665); a synthetic adrenocorticosteroid that acts as an anti-inflammatory and anti-pruritic agent. It is used as a topical for the treatment of dermatologic disorders such as atopic dermatitis and psoriasis.

Check Digit Verification of cas no

The CAS Registry Mumber 6677-98-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,7 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6677-98:
(6*6)+(5*6)+(4*7)+(3*7)+(2*9)+(1*8)=141
141 % 10 = 1
So 6677-98-1 is a valid CAS Registry Number.
InChI:InChI=1/C24H34O6/c1-4-20(28)30-13-19(27)24(29)10-8-17-16-6-5-14-11-15(25)7-9-22(14,2)21(16)18(26)12-23(17,24)3/h11,16-18,21,26,29H,4-10,12-13H2,1-3H3/t16-,17-,18-,21+,22-,23-,24-/m0/s1

6677-98-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 21-oxopropoxy-11β,17α-dihydroxypregn-4-ene-3,20-dione

1.2 Other means of identification

Product number -
Other names hydrocortisone propionate

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:6677-98-1 SDS

6677-98-1Upstream product

6677-98-1Downstream Products

6677-98-1Relevant articles and documents

Process for preparing 3-enol ethers of 11β-hydroxy-Δ4 -pregnene-3-ones and derivatives thereof

-

, (2008/06/13)

3-enol ethers of 11β-hydroxy-Δ4 -pregnene-3-ones are prepared by reacting triethylorthoacetate with an 11β-hydroxy-Δ4 -pregnene-3-one in a solvent which is at least 40% by weight or more ethanol and 60% by weight or less of a compatible oxygenated hydrocarbon liquid in the presence of an acid catalyst. This reaction forms a basis of a process for forming 6-halo-derivatives, particularly 6-chloro-Δ1,4,6 -pregnatrien -11β,17α,21-triol-3,20-dione.

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