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54433-86-2

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54433-86-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54433-86-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,4,3 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 54433-86:
(7*5)+(6*4)+(5*4)+(4*3)+(3*3)+(2*8)+(1*6)=122
122 % 10 = 2
So 54433-86-2 is a valid CAS Registry Number.

54433-86-2SDS

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 1,3a<sup>1</sup>-dihydroxy-3a,5,5,8-tetramethyldecahydro-1H-cyclopenta[de]isochromen-6-yl acetate

1.2 Other means of identification

Product number -
Other names -

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:54433-86-2 SDS

54433-86-2Relevant articles and documents

Botrylactone: New interest in an old molecule - Review of its absolute configuration and related compounds

Moraga, Javier,Pinedo, Cristina,Durán-Patrón, Rosa,Collado, Isidro G.,Hernández-Galán, Rosario

experimental part, p. 417 - 420 (2011/03/19)

The absolute configuration of botrylactone, a unique compound with an interesting polyketide lactone skeleton with two oxirane bridges previously isolated from Botrytis cinerea and described as a powerful antibiotic, has been reviewed on the basis of sign of the optical rotation, NOE experiments and NMR method. The isolation of 7-deoxybotrylactone and 5-hydroxy-7-(4-hydroxydec-2(3)- enoyl) botrylactone enables us to characterize an intriguing new family of compounds with this interesting polyketide skeleton. A common biosynthetic origin with botcinin derivatives is proposed. Copyright

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