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7392-19-0

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7392-19-0 Usage

Description

LIMETOL is a cyclized derivative of linalool, melanol, and other unsaturated alcohols, which is used in the fragrance and perfumery industry.

Uses

Used in Fragrance and Perfumery Industry:
LIMETOL is used as a fragrance ingredient for its unique scent and ability to enhance the overall aroma of perfumes and fragrances. Its cyclized structure provides a distinct and long-lasting scent, making it a valuable addition to the fragrance industry.

Check Digit Verification of cas no

The CAS Registry Mumber 7392-19-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,9 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7392-19:
(6*7)+(5*3)+(4*9)+(3*2)+(2*1)+(1*9)=110
110 % 10 = 0
So 7392-19-0 is a valid CAS Registry Number.
InChI:InChI=1S/C10H18O/c1-5-10(4)8-6-7-9(2,3)11-10/h5H,1,6-8H2,2-4H3

7392-19-0SDS

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 LIMETOL

1.2 Other means of identification

Product number -
Other names 2-ethynyl-2,6,6-trimethyltetrahydro-2H-pyran

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:7392-19-0 SDS

7392-19-0Relevant articles and documents

Amberlyst-15-catalyzed efficient cyclization of γ-and δ-unsaturated alcohols: Green synthesis of oxygen heterocycles

Singh, Soni A.,Kabiraj, Shilpi,Khandare, Reena P.,Nalawade, Shrikant P.,Upar, Kiran B.,Bhat, Sujata V.

experimental part, p. 74 - 80 (2010/03/24)

Amberlyst-15 (H+) resin catalyzes efficient cationic endo-cyclization of-and-unsaturated alcohols to yield tetrahydro-(2H)-pyrans and oxepanes. The merits of the present protocol are good yield of the products under mild conditions, simple workup, and reusability of the resin.

A PRACTICAL SYNTHESIS OF MYRCENOL BY PALLADIUM COMPLEX-CATALYZED ELIMINATION REACTION

Kumobayashi, Hidenori,Mitsuhashi, Shigeru,Akutagawa, Susumu,Ohtsuka, Sei

, p. 157 - 160 (2007/10/02)

A Palladium complex-catalyzed elimination reaction of allyl amines was studied to establish a practical process for production of myrcenol.The catalytic elimination occurred smoothly with the cationic Pd(II) complexes.Among a variety phosphorous ligands, the tetramethylene and the pentamethylene diphosphine ligands proved to be the best ligand with respects to the catalytic activity and selectivity.

Cyclisation des alcools δ-alleniques par le nitrate d'argent ou les sels mercuriques. Synthese d'α-alcenyl-2 tetrahydropyrannes

Audin, Patrick,Doutheau, Alain,Gore, Jacques

, p. 297 - 306 (2007/10/02)

Eight diversely substituted δ-allenic alcohols have been synthesized by using three different methods for the formation of the allenic linkage.When treated with silver nitrate or mercuric salts, these alcohols are transformed in fairly good yields into α-alkenyl-2 tetrahydropyrans.In addition to its regioselectivity in the formation of the heterocycle this reaction shows in certain cases a high stereoselectivity.Alcohols monosubstituted on the thermal allenic carbon lead to more than 90percent of the E product whereas the 2,4 or 2,6 disubstituted tetrahydropyrans are obtained in predominantly the Z configuration.

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