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111465-42-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111465-42-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,4,6 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 111465-42:
90 % 10 = 0
So 111465-42-0 is a valid CAS Registry Number.



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


1.1 GHS Product identifier

Product name (3S,4R,9R)-9-ethyl-3-(hydroxymethyl)-1,7-dioxaspiro[5.5]undecan-4-ol

1.2 Other means of identification

Product number -
Other names Talaromycin E

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:111465-42-0 SDS

111465-42-0Relevant articles and documents

Talaromycins: Applications of Homonuclear Spin Correlation Maps to Structure Assignements

Lynn, David G.,Phillips, Nancy J.,Hutton, William C.,Shabanowitz, Jeffrey,Fennell, D. I.,Cole, R. J.

, p. 7319 - 7322 (1982)


Enantioselective Total Synthesis of the Mycotoxin (-)-Talaromycin B by a Hetero Diels-Alder Reaction

Tietze, Lutz F.,Schneider, Christoph

, p. 2476 - 2481 (2007/10/02)

(-)-Talaromycin B was formed in an overall yield of 5 percent in nine steps via a hetero Diels-Alder reaction of the exocyclic vinyl ether 3 and methyl O-benzoyldiformylacetate (4) as the key transformation.The enantiomerically pure vinyl ether 3 was prep


Mori, Kenji,Ikunaka, Masaya

, p. 45 - 58 (2007/10/02)

Highly enantiomerically pure (-)-talaromycins A and B undecane> were synthesized starting from chiral building blocks of microbial origin.

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