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86578-99-6

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86578-99-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86578-99-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,5,7 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 86578-99:
(7*8)+(6*6)+(5*5)+(4*7)+(3*8)+(2*9)+(1*9)=196
196 % 10 = 6
So 86578-99-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H20O2/c1-11-9-7-5-3-2-4-6-8-10-12(13)14-11/h6,8,11H,2-5,7,9-10H2,1H3/b8-6-/t11-/m0/s1

86578-99-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (3Z,11S)-(+)-3-dodecen-11-olide

1.2 Other means of identification

Product number -
Other names ferrulactone II

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:86578-99-6 SDS

86578-99-6Downstream Products

86578-99-6Relevant articles and documents

Chemoenzymatic synthesis of ferrulactone II and (2E)-9-hydroxydecenoic acid

Pawar,Sankaranarayanan,Chattopadhyay

, p. 2219 - 2226 (2007/10/03)

A novel and divergent synthesis of the title compounds has been developed. The salient features of the synthesis were use of easily accessible starting material, regioselective organometallic reaction and enzymatic derivation of the key synthons.

Synthesis of Four Macrolide Pheromones to Define the Scope and Limitation of Enzymatic Macrolactonization

Mori, Kenji,Tomioka, Hiroki

, p. 1011 - 1018 (2007/10/02)

The macrolides, (R)-ferrulactone II (2), (Z)-3-dodecen-12-olide (3) and (5Z,13R)-5-tetradecen-13-olide (4), could be synthesized by enzymatic macrolactonization with lipases by starting from (+/-)-12, 17 and (+/-)-24, respectively.Ferrulactone I (1) was p

THERMOSTABLE ENZYMES IN ORGANIC SYNTHESIS, 5. TOTAL SYNTHESIS OF S-(+)-Z-DODEC-3-EN-11-OLIDE (FERRULACTONE II) USING A TBADH-GENERATED BIFUNCTIONAL CHIRON.

Keinan, Ehud,Sinha, Subhash C.,Singh, Surendra P.

, p. 4631 - 4638 (2007/10/02)

The total synthesis of (S)-(+)-ferrulactone (2), one of several synergistic aggregation pheromones produced by male flat grain beetles, Cryptolestes ferrugineus (Stephens) was achieved in a five-step synthesis in very high optical purity (>99percent ee) a

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