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18045-83-5

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  • Cyclodeca[b]furan-2(3H)-one,3a,4,5,8,9,11ahexahydro- 9-hydroxy-6,10-dimethyl-3- methylene-,(3aS,6E,9R,10E,11aR)-

    Cas No: 18045-83-5

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  • Cyclodeca[b]furan-2(3H)-one,3a,4,5,8,9,11ahexahydro- 9-hydroxy-6,10-dimethyl-3- methylene-,(3aS,6E,9R,10E,11aR)- cas 18045-83-5

    Cas No: 18045-83-5

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18045-83-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18045-83-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,4 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 18045-83:
(7*1)+(6*8)+(5*0)+(4*4)+(3*5)+(2*8)+(1*3)=105
105 % 10 = 5
So 18045-83-5 is a valid CAS Registry Number.
InChI:InChI=1/C15H20O3/c1-9-4-6-12-11(3)15(17)18-14(12)8-10(2)13(16)7-5-9/h5,8,12-14,16H,3-4,6-7H2,1-2H3/b9-5-,10-8+

18045-83-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (6Z,10E)-9-hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one

1.2 Other means of identification

Product number -
Other names Tamaulipin B

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:18045-83-5 SDS

18045-83-5Downstream Products

18045-83-5Relevant articles and documents

Stereo-controlled Alkylation of Cyclodecadienone Derivatives and the Total Synthesis of (-)- and (+)-4,5-cis-3β-Hydroxygermacranolides

Nakamura, Takayoshi,Hirota, Hiroshi,Kuroda, Chiaki,Takahashi, Takeyoshi

, p. 1879 - 1882 (2007/10/02)

Direct trapping of the intermediate, produced by anionic oxy-Cope rearrangement of (1S,4S,6S)-4-alkoxy-1-ethenyl-3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-ol, with ethyl bromoacetate gave ethyl -3-alkoxy-6-oxo-13-nor-1(10),4-germacradien-12-oate stereoselectively, which was converted into a natural (-)-4,5-cis-3β-hydroxygermacranolide.

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