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5-(2,2,3-trimethyl-3-cyclopenten-1-yl)pent-4-en-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55730-89-7

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55730-89-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55730-89-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,3 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 55730-89:
(7*5)+(6*5)+(5*7)+(4*3)+(3*0)+(2*8)+(1*9)=137
137 % 10 = 7
So 55730-89-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H20O/c1-10-8-9-12(13(10,3)4)7-5-6-11(2)14/h5,7-8,12H,6,9H2,1-4H3

55730-89-7SDS

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 5-(2,2,3-trimethylcyclopent-3-en-1-yl)pent-4-en-2-one

1.2 Other means of identification

Product number -
Other names EINECS 259-781-3

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:55730-89-7 SDS

55730-89-7Downstream Products

55730-89-7Relevant academic research and scientific papers

(2R*,3S*)-(E)-3-methyl-5-(2,2,3-trimethylcyclopent-3-en-1-yl)pent-4-en-2-ol

-

, (2008/06/13)

(2R*,3S*)-(E)-3-Methyl-5-(2,2,3-trimethylcyclopent-3-en-1-yl)pent-4-en-2-ol possesses a very intense creamy, woody, musk, sandalwood odor and is a valuable ingredient for use in fragrance compositions for its musk and sandalwood-like qualities. This odorant is more intense than any of the campholenic aldehyde derivatives that have been previously reported.

Insect Growth Regulators. XIII - Juvenoids with Cyclopentene Ring. Synthesis of Alkyl ω-(2,2,3-Trimethyl-Cyclopent-3-en-1-yl)-2-alkenoates and ω-(2,2,3-Trimethyl-Cyclopent-3-en-1-yl)alkyl Phenyl Ethers

Derdzinski, K.,Wawrzenczyk, C.,Zabza, A.,et al.

, p. 196 - 212 (2007/10/02)

Neue Analoga der Insektenjuvenilhormone mit dem Cyclopentenring wurden aus dem (2,2,3-Trimethyl-cyclopent-3-en-1-yl)acetonitril (1) durch eine mehrstufige Synthese erhalten.Die Ether 7a-c, 8a, b, 15a-c und 34a, b wurden durch Alkylierung der 4-substituierten Phenolate mit entsprechenden Tosylaten oder Bromiden synthetisiert.Die Ester 11a-c, 12a, b, 21a-c, 23a-c, 28a, b, 29, 27 und 33a, b mit unterschiedlicher Kettenlaenge wurden durch die Wadsworth-Emmons-Reaktion der Ketone 11, 12, 19, 26, 27, 32 bzw. des Aldehydes 16 mit entsprechenden Phosphonsaeurealkylestern erhalten.

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