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(2R,8aβ)-Decahydro-α,α,4aα,8α-tetramethylnaphthalene-2α-methanol is a complex organic compound with a molecular formula of C15H26O. It is a stereoisomer of decahydro-tetramethylnaphthalene, characterized by its unique molecular structure and chiral centers. (2R,8aβ)-Decahydro-α,α,4aα,8α-tetramethylnaphthalene-2α-methanol is a type of bicyclic hydrocarbon, specifically a naphthalene derivative, with four methyl groups attached to the carbon atoms. The presence of the hydroxyl group (-OH) at the 2α position indicates that it is an alcohol. This chemical is of interest in organic chemistry due to its potential applications in the synthesis of various pharmaceuticals and fragrances, as well as its role as an intermediate in the production of other organic compounds. Its specific stereochemistry, indicated by the (2R,8aβ) notation, is crucial for its reactivity and potential applications, as different stereoisomers can have significantly different properties and uses.

6770-16-7

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6770-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6770-16-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,7 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6770-16:
(6*6)+(5*7)+(4*7)+(3*0)+(2*1)+(1*6)=107
107 % 10 = 7
So 6770-16-7 is a valid CAS Registry Number.

6770-16-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name dihydroeudesmol

1.2 Other means of identification

Product number -
Other names Dihydroeudesmol

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:6770-16-7 SDS

6770-16-7Relevant academic research and scientific papers

Structures and spasmolytic activities of derivatives from sesquiterpenes of Alpinia speciosa and Alpinia japonica

Morita, Makoto,Nakanishi, Hiroshi,Morita, Hiroshi,Mihashi, Susumu,Itokawa, Hideji

, p. 1603 - 1606 (2007/10/03)

Sesquiterpenes isolated from Alpinia speciosa and Alpinia japonica, and their derivatives were found to inhibit histamine- or barium chloride- induced contraction of excised guinea pig ileum when tested by the Magnus method. Major spasmolytic principles contained in those extracts were the sesquiterpenes, β-eudesmol, nerolidol, humulene epoxide II and 4α- hydroxydihydroagarofuran. Relationships between the chemical structures of the sesquiterpenes and their derivatives, and their spasmolytic activities were discussed.

TERPENOIDS FROM PLANTS OF THE FAMILY CUPRESSACEAE. SESQUITERPENE ALCOHOLS FROM THE NEEDLES OF Microbiota decussata

Raldugin, V. A.,Storozhenko, V. G.,Rezvukhin, A. I.,Pentegova, V. A.,Gorovoi, P. G.,Baranov, V. I.

, p. 124 - 129 (2007/10/02)

The sesquiterpene alcohols 5S,8S-germacra-1E,6E-dien-5-ol, (+)-α-bisabolol, hedycaryol, and β-eudesmol and also the previously undescribed alcohols thujopsan-2α-ol (I) and microbiotol.Microbiotol is a tricyclic tertiary alcohol with the empirical formula C15H26O, mp 112-113 deg C, containing in its molecule four tertiary methyl groups and cyclopropane ring.

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