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(3aR,8aS)-2,2,8-trimethyl-3,3a,6,8a-tetrahydro-1H-azulene-5,6-dicarbaldehyde is a complex chemical compound characterized by its tetrahydroazulene core and two aldehyde groups. This highly aromatic compound is known for its distinct odor, making it a valuable component in the fragrance industry.

50656-61-6

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50656-61-6 Usage

Uses

Used in Fragrance Industry:
(3aR,8aS)-2,2,8-trimethyl-3,3a,6,8a-tetrahydro-1H-azulene-5,6-dicarbaldehyde is used as a fragrance ingredient for its unique and distinct scent. It contributes to the overall scent profile of perfumes and other fragranced products, enhancing their appeal and longevity.
Used in Organic Synthesis:
(3aR,8aS)-2,2,8-trimethyl-3,3a,6,8a-tetrahydro-1H-azulene-5,6-dicarbaldehyde may have potential applications in organic synthesis due to its complex structure and functional groups. Its use in this field could lead to the development of new compounds and materials with various properties and applications.
Used in Medicinal Chemistry:
Although further research is needed, (3aR,8aS)-2,2,8-trimethyl-3,3a,6,8a-tetrahydro-1H-azulene-5,6-dicarbaldehyde may also find potential use in medicinal chemistry. Its unique structure and functional groups could be harnessed for the development of new pharmaceutical compounds with potential therapeutic benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 50656-61-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,5 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 50656-61:
(7*5)+(6*0)+(5*6)+(4*5)+(3*6)+(2*6)+(1*1)=116
116 % 10 = 6
So 50656-61-6 is a valid CAS Registry Number.
InChI:InChI=1/C15H20O2/c1-10-4-12(8-16)13(9-17)5-11-6-15(2,3)7-14(10)11/h4-5,8-9,11-12,14H,6-7H2,1-3H3/t11-,12?,14-/m1/s1

50656-61-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,8-trimethyl-3,3a,6,8a-tetrahydro-1H-azulene-5,6-dicarbaldehyde

1.2 Other means of identification

Product number -
Other names -

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:50656-61-6 SDS

50656-61-6Downstream Products

50656-61-6Relevant academic research and scientific papers

Stereostructure of plagiochiline A and conversion of plagiochiline A and stearoylvelutinal into hot-tasting compounds by human saliva

Hashimoto,Tanaka,Asakawa

, p. 1542 - 1544 (1994)

The stereostructure of plagiochiline A (1) isolated from the liverwort Plagiochila fruticosa has been established by X-ray crystallographic analysis. Plagiochiline A was converted into plagiochilal B (2) and furanoplagiochilal (3) by human saliva, and stearoylvelutinal (4) isolated from the fungus Lactarius vellerus was converted into velleral (5), also by human saliva.

NEW SESQUITERPENES IN A PROPOSED RUSSULACEAE CHEMICAL DEFENSE SYSTEM

Sterner, Olov,Bergman, Rolf,Franzen, Claes,Wickberg, Boerje

, p. 3163 - 3166 (2007/10/02)

In addition to already known sesquiterpene aldehydes, the lactaranes piperdial 1 and piperalol 2 were isolated from extracts of Lactarius piperatus, L. torminosus and Russula queletii (larger fungi).

VELUTINAL ESTERS OF LACTARIUS VELLEREUS AND L. NECATOR. THE PREPARATION OF FREE VELUTINAL.

Sterner, Olov,Bergman, Rolf,Kesler, Ewa,Nilsson, Liselott,Oluwadiya, James,Wickberg, Boerje

, p. 1415 - 1418 (2007/10/02)

Esters of the pentacyclic sesquiterpene velutinal have been isolated from Lactarius species, and converted to the free alcohol by base-catalyzed transesterification in EtOH/EtO(1-).

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