Welcome to LookChem.com Sign In|Join Free
  • or
(3S)-5β,6α,7α-Triacetoxy-3aα,4,4a,5,6,7,7aα,8,9,9aα-decahydro-3β,4aβ,8α-trimethylazuleno[6,5-b]furan-2(3H)-one is a complex cyclic terpene derivative of azulene, characterized by a furan ring and a decalin system. It is a natural organic compound with potential applications in various industries due to its unique chemical structure and properties.

62121-29-3

Post Buying Request

62121-29-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

62121-29-3 Usage

Uses

Used in the Fragrance Industry:
(3S)-5β,6α,7α-Triacetoxy-3aα,4,4a,5,6,7,7aα,8,9,9aα-decahydro-3β,4aβ,8α-trimethylazuleno[6,5-b]furan-2(3H)-one is used as a key ingredient in the fragrance industry for its unique scent and ability to enhance the aroma of perfumes and other scented products. Its complex structure contributes to a distinct and long-lasting fragrance.
Used in the Flavor Industry:
In the flavor industry, (3S)-5β,6α,7α-Triacetoxy-3aα,4,4a,5,6,7,7aα,8,9,9aα-decahydro-3β,4aβ,8α-trimethylazuleno[6,5-b]furan-2(3H)-one is used as an additive to impart specific flavors to various food and beverage products. Its unique chemical composition allows it to contribute to the overall taste profile of these products.
Used in the Pharmaceutical Industry:
(3S)-5β,6α,7α-Triacetoxy-3aα,4,4a,5,6,7,7aα,8,9,9aα-decahydro-3β,4aβ,8α-trimethylazuleno[6,5-b]furan-2(3H)-one is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a valuable component in the development of new drugs and medications.
Used in Organic Chemistry Research:
In the field of organic chemistry, (3S)-5β,6α,7α-Triacetoxy-3aα,4,4a,5,6,7,7aα,8,9,9aα-decahydro-3β,4aβ,8α-trimethylazuleno[6,5-b]furan-2(3H)-one serves as a model compound for studying the properties and reactivity of complex cyclic terpenes. Its structure provides insights into the behavior of similar compounds and aids in the development of new synthetic methods and strategies.
Used in Medicinal Chemistry Research:
(3S)-5β,6α,7α-Triacetoxy-3aα,4,4a,5,6,7,7aα,8,9,9aα-decahydro-3β,4aβ,8α-trimethylazuleno[6,5-b]furan-2(3H)-one is also used in medicinal chemistry research for its potential therapeutic applications. Its unique chemical structure may offer new avenues for the development of novel drugs and treatments for various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 62121-29-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,2 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 62121-29:
(7*6)+(6*2)+(5*1)+(4*2)+(3*1)+(2*2)+(1*9)=83
83 % 10 = 3
So 62121-29-3 is a valid CAS Registry Number.
InChI:InChI=1/C21H30O8/c1-9-7-15-14(10(2)20(25)29-15)8-21(6)16(9)17(26-11(3)22)18(27-12(4)23)19(21)28-13(5)24/h9-10,14-19H,7-8H2,1-6H3/t9-,10+,14-,15-,16-,17-,18-,19+,21+/m1/s1

62121-29-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [(1S,3aR,5R,5aS,6R,7R,8R,8aS,9aR)-7,8-diacetyloxy-1,5,8a-trimethyl-2-oxo-1,3a,4,5,5a,6,7,8,9,9a-decahydroazuleno[6,5-b]furan-6-yl] acetate

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:62121-29-3 SDS

62121-29-3Upstream product

62121-29-3Downstream Products

62121-29-3Relevant academic research and scientific papers

Sesquiterpene Lactones of Hymenoxys insignis. X-ray Analyses of Hymenograndin and Hymenosignin

Herz, Werner,Govindan, S.V.,Bierner, Mark W.,Blount, John F.

, p. 493 - 497 (1980)

Hymenoxys insignis yielded the new guaianolide hymenosignin (2) and the new helenanolide acetylhymenograndin (3b).The structures were established by physical methods.These included X-ray analyses of 2 and hymenograndin (3a), whose previously postulated stereochemistry at C-2 and C-3 was found to require revision.Conformations of the various compounds and their bearings on the CD curves of substances related to 3a,b are discussed, and a suggestion is made to account for the co-occurrence of hymenosignin and acetylhymenograndin.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 62121-29-3