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4029-65-6

4029-65-6

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  • 5-[(5R,8R,9S,10S,13R,14S,17S)-14-hydroxy-10,13-dimethyl-3-oxo-2,4,5,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]pyran-2-one

    Cas No: 4029-65-6

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  • 5-[(5R,8R,9S,10S,13R,14S,17S)-14-hydroxy-10,13-dimethyl-3-oxo-2,4,5,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]pyran-2-one cas 4029-65-6

    Cas No: 4029-65-6

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4029-65-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4029-65-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,2 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4029-65:
(6*4)+(5*0)+(4*2)+(3*9)+(2*6)+(1*5)=76
76 % 10 = 6
So 4029-65-6 is a valid CAS Registry Number.
InChI:InChI=1/C24H32O4/c1-22-10-7-17(25)13-16(22)4-5-20-19(22)8-11-23(2)18(9-12-24(20,23)27)15-3-6-21(26)28-14-15/h3,6,14,16,18-20,27H,4-5,7-13H2,1-2H3/t16-,18-,19+,20-,22+,23-,24+/m1/s1

4029-65-6SDS

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 Bufalone

1.2 Other means of identification

Product number -
Other names 3-keto-bufalin

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:4029-65-6 SDS

4029-65-6Upstream product

4029-65-6Downstream Products

4029-65-6Relevant articles and documents

Bufalin riboside having selective inhibition action to Na+/K+-ATPase alpha2 subtype and application of bufalin riboside

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Paragraph 0036; 0037, (2016/12/07)

The invention belongs to the technical field of preparation of cardiotonic drugs, and discloses bufalin riboside having selective inhibition action to Na+/K+-ATPase alpha2 subtype and an application of the bufalin riboside. The structural formula of the bufalin riboside is as shown in the formula (I).Synthesis of the bufalin riboside is carried out for the first time. The bufalin riboside is high in safety and high in cardiotonic effect, can be prepared into different form of drugs, has good medicinal prospect, has the advantages of preparation simplicity, low cost and high productivity; and its selectivity to alpha1 and alpha2 subtypes is up to 17.0.

Transformation of digitoxigenin to scillarenin.

Kamano,Pettit

, p. 8592 - 8593 (2007/10/10)

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