+1 858-523-8231
Login | Register
AA Blocks, Building Blocks, Catalysts, Inhibitors
Login | Register
Home Other Building Blocks 6790-58-5
6790-58-5,MFCD00134491
Catalog No.:AA0062GB

6790-58-5 | (-)-Ambroxide

Pack Size
Purity
Availability
Price(USD)
Quantity
  
25mg
97%
in stock  
$7.00   $5.00
- +
1g
98%
in stock  
$18.00   $13.00
- +
5g
97%
in stock  
$35.00   $25.00
- +
25g
97%
in stock  
$111.00   $78.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA0062GB
Chemical Name:
(-)-Ambroxide
CAS Number:
6790-58-5
Molecular Formula:
C16H28O
Molecular Weight:
236.3929
MDL Number:
MFCD00134491
SMILES:
CC1(C)CCC[C@]2([C@H]1CC[C@@]1([C@@H]2CCO1)C)C
Properties
Properties
 
Form:
Solid  
MP:
74-76 °C(lit.)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
322  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
4  
Heavy Atom Count:
17  
Hydrogen Bond Acceptor Count:
1  
XLogP3:
4.7  

Downstream Synthesis Route

[1]SyntheticCommunications,2001,vol.31,p.749-758

[2]TetrahedronLetters,1993,vol.34,p.629-632

[3]BulletindelaSocieteChimiquedeFrance,1997,vol.134,p.1001-1024

[4]SyntheticCommunications,2004,vol.34,p.3631-3643

[5]TetrahedronLetters,1988,vol.29,p.1017-1020

[6]Tetrahedron,2001,vol.57,p.5657-5662

[7]Patent:CN105017191,2017,B.Locationinpatent:Paragraph0033-0034

[8]TetrahedronAsymmetry,1998,vol.9,p.3819-3823

[9]Tetrahedron,2002,vol.58,p.5941-5949

[10]BioorganicandMedicinalChemistryLetters,2015,vol.25,p.2773-2777

[11]HelveticaChimicaActa,1985,vol.68,p.2022-2029

[12]TetrahedronAsymmetry,1996,vol.7,p.1695-1704

[13]BulletindelaSocieteChimiquedeFrance,1997,vol.134,p.1001-1024

[14]Tetrahedron,1993,vol.49,p.10405-10412

[15]Patent:US4503240,1985,A

[16]Patent:WO2009/10791,2009,A2.Locationinpatent:Page/Pagecolumn9;10;12;13

[17]Patent:WO2009/10791,2009,A2.Locationinpatent:Page/Pagecolumn10;13

[18]Patent:WO2009/10791,2009,A2.Locationinpatent:Page/Pagecolumn10;12;13

[19]Patent:WO2013/7832,2013,A1.Locationinpatent:Page/Pagecolumn45;46

[20]Patent:US2019/23679,2019,A1.Locationinpatent:Paragraph0058;0059

[1]Tetrahedron,1988,vol.44,p.1925-1932

[1]Tetrahedron,1988,vol.44,p.1925-1932

[1]Tetrahedron,1993,vol.49,p.6251-6262

[2]Tetrahedron,1993,vol.49,p.9525-9534

[1]Tetrahedron,1994,vol.50,p.10095-10106

Literature

Title: Isolation, chemical, and biotransformation routes of labdane-type diterpenes.

Journal: Chemical reviews 20110810

Title: Antibacterial and cytotoxic activity of the acetone extract of the flowers of Salvia sclarea and some natural products.

Journal: Pakistan journal of pharmaceutical sciences 20070401

Title: Chiral decalins: preparation from oleanolic acid and application in the synthesis of (-)-9-epi-ambrox.

Journal: Journal of natural products 20061101

Title: Biotransformation of (-)-ambrox by cell suspension cultures of Actinidia deliciosa.

Journal: Journal of natural products 20060601

Title: Enantio- and diastereoselective stepwise cyclization of polyprenoids induced by chiral and achiral LBAs. A new entry to (-)-ambrox, (+)-podocarpa-8,11,13-triene diterpenoids, and (-)-tetracyclic polyprenoid of sedimentary origin.

Journal: Journal of the American Chemical Society 20020410

Title: Zerbe P, et al. Enzymes for synthetic biology of ambroxide-related diterpenoid fragrance compounds. Adv Biochem Eng Biotechnol. 2015;148:427-47.

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Related Products of 6790-58-5
15536-71-7

15536-71-7

 23377-40-4

23377-40-4

 278-74-0

278-74-0

 286-20-4

286-20-4

 286-45-3

286-45-3

 286-62-4

286-62-4
Building Blocks
More >
Tags:6790-58-5 Molecular Formula|6790-58-5 MDL|6790-58-5 SMILES|6790-58-5 (-)-Ambroxide |Heterocyclic_Building_Blocks