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36025-82-8

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36025-82-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36025-82-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,0,2 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 36025-82:
(7*3)+(6*6)+(5*0)+(4*2)+(3*5)+(2*8)+(1*2)=98
98 % 10 = 8
So 36025-82-8 is a valid CAS Registry Number.

36025-82-8SDS

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 3-oxoandrost-4-en-17α-yl benzoate

1.2 Other means of identification

Product number -
Other names testosterone 17α-benzoate

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:36025-82-8 SDS

36025-82-8Relevant articles and documents

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Loibner,H.,Zbiral,E.

, p. 417 - 425 (1977)

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Structure-based design and synthesis of novel potent Na+,K +-ATPase inhibitors derived from a 5α,14α-androstane scaffold as positive inotropic compounds

De Munari, Sergio,Cerri, Alberto,Gobbini, Mauro,Almirante, Nicoletta,Banfi, Leonardo,Carzana, Giulio,Ferrari, Patrizia,Marazzi, Giuseppe,Micheletti, Rosella,Schiavone, Antonio,Sputore, Simona,Torri, Marco,Zappavigna, Maria Pia,Melloni, Piero

, p. 3644 - 3654 (2007/10/03)

The design, synthesis, and biological properties of novel inhibitors of the Na+,K+-ATPase as potential positive inotropic compounds are reported. Following our model of superposition between cassaine and digitoxigenin, digitalis-like

Efficacious modification of the Mitsunobu reaction for inversions of sterically hindered secondary alcohols

Martin,Dodge

, p. 3017 - 3020 (2007/10/02)

A practical modification of the Mitsunobu protocol for effecting stereochemical inversions of alcohols has been discovered in which use of p-nitrobenzoic acid as the nucleophilic partner results in significantly improved yields with relatively hindered su

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