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571-25-5

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571-25-5 Usage

Uses

(17β)?-?17-?Hydroxyandrost-?5-?en-?3-?one is a reagent in the synthesis of new hedgehog signaling inhibitors which may be used in cancer treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 571-25-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,7 and 1 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 571-25:
(5*5)+(4*7)+(3*1)+(2*2)+(1*5)=65
65 % 10 = 5
So 571-25-5 is a valid CAS Registry Number.

571-25-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (17β)-17-Hydroxyandrost-5-en-3-one

1.2 Other means of identification

Product number -
Other names 5-Amyl-thienyl(2)acrylsaeure

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:571-25-5 SDS

571-25-5Upstream product

571-25-5Relevant articles and documents

o-Nitrophenylethylene glycol as photoremovable protective group for aldehydes and ketones: syntheses, scope, and limitations

Gravel, D.,Herbert, J.,Thoraval, D.

, p. 400 - 410 (2007/10/02)

The preparation of o-nitophenylethylene glycol is described along with its application as a photolabile protective group for aldehydes and ketones.Formation of the acetals and ketals is achieved in good to high yields in the usual manner and deprotection is carried out in fair to high yield, by photolysis at 350 nm in an inert solvent such as benzene.Because of the particular nature of the present protective group, its stability to basic and acidic conditions has been examined and is reported to complete the scope and limitations aspect.From a mechanistic point of view, the isolation and characterisation of o-nitroso-α-hydroxyacetophenone as the spent reagent demonstrates a mechanistic link with the known o-nitrobenzaeldehyde to o-nitrobenzoic acid photorearrangement.

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