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19069-48-8

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19069-48-8 Usage

Type of compound

Polycyclic hydrocarbon

Primary use

Production of fragrances and flavorings

Structure

Unique tricyclic structure with four methyl groups attached to carbon atoms

Physical state

Colorless liquid

Odor

Strong, floral

Use in perfumes

Ideal ingredient due to its odor

Use as synthetic intermediate

Production of various other organic compounds

Demand

High in the fragrance and flavor industry due to its aromatic properties and versatile applications.

Check Digit Verification of cas no

The CAS Registry Mumber 19069-48-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,6 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19069-48:
(7*1)+(6*9)+(5*0)+(4*6)+(3*9)+(2*4)+(1*8)=128
128 % 10 = 8
So 19069-48-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H24/c1-10-7-8-15-9-12(10)14(3,4)13(15)6-5-11(15)2/h7,11-13H,5-6,8-9H2,1-4H3/t11-,12?,13?,15?/m1/s1

19069-48-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6,6,8-TETRAMETHYLTRICYCLO[5.3.1.0(1,5)]UNDEC-8-ENE

1.2 Other means of identification

Product number -
Other names Urabaine

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:19069-48-8 SDS

19069-48-8Relevant articles and documents

Synthetic Studies on Arene-Olefin Cycloadditions: Total Synthesis of (+/-)-α-Cedrene

Wender, P. A.,Howbert, J. J.

, p. 688 - 690 (1981)

-

Bang et al.

, p. 2087,2089,2090,2093 (1973)

Total synthesis of α-cedrene: A new strategy utilizing N- aziridinylimine radical chemistry

Lee, Hee-Yoon,Lee, Sejin,Kim, Deogil,Kim, Byung Kyu,Bahn, Jong Soo,Kim, Sunggak

, p. 7713 - 7716 (2007/10/03)

Tandem free radical cycloaddition reaction of the N-Aziridinylimine intermediate produced tricyclo[5.3.1.01,5]undecane skeleton stereoselectively. A total synthesis of α-cedrene was completed in three step sequence from the cyclization product.

THE DIRECT CONVERSION OF EPOXIDES INTO ALKENES via IODOHYDRINS BY in situ GENERATED HI

Garlaschelli, Luigi,Vidari, Giovanni

, p. 251 - 254 (2007/10/02)

Epoxides are easily converted into iodohydrins and alkenes are obtained from either epoxides or iodohydrins by treatment with HI, generated in situ from Ph3P*I2 in moist CH3CN.

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