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(1R,2S,5R)-6-Methylene-2-[(3aS)-octahydro-4,7aα-dimethyl-1,3-dioxoisobenzofuran-4α-yl]bicyclo[3.2.1]octane-1-carbaldehyde is a complex organic compound with a molecular formula of C17H24O4. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it possesses three chiral centers (1R, 2S, and 5R). The compound features a bicyclo[3.2.1]octane core, which is a type of bicyclic structure consisting of two fused rings with a total of eight carbon atoms. Additionally, it contains a methylene group (-CH2-), an isobenzofuran ring, and a carbaldehyde functional group. The isobenzofuran ring is a heterocyclic compound with a benzene ring fused to a furan ring, and the carbaldehyde group is an aldehyde with a carbonyl group (C=O) at the end of a carbon chain. (1R,2S,5R)-6-Methylene-2-[(3aS)-octahydro-4,7aα-dimethyl-1,3-dioxoisobenzofuran-4α-yl]bicyclo[3.2.1]octane-1-carbaldehyde is likely to be found in the field of organic chemistry, potentially as a synthetic intermediate or a component in the synthesis of natural products.

6750-11-4

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6750-11-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6750-11-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,5 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6750-11:
(6*6)+(5*7)+(4*5)+(3*0)+(2*1)+(1*1)=94
94 % 10 = 4
So 6750-11-4 is a valid CAS Registry Number.

6750-11-4SDS

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 fujenal

1.2 Other means of identification

Product number -
Other names ent-7-Oxo-6,7-secokaur-16-en-6,19-dicarbonsaeureanhydrid

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:6750-11-4 SDS

6750-11-4Relevant academic research and scientific papers

THE MICROBIOLOGICAL TRANSFORMATION OF SOME ENT-KAUR-16-ENE 7-, 15- AND 18-ALCOHOLS BY GIBBERELLA FUJIKUROI

Fraga, Braulio M.,Hanson, James R.,Hernandez, Melchior G.,Sarah, Fahmi Y.

, p. 1087 - 1092 (1980)

The effect of the 7-, 15- and 18-hydroxyl groups on the microbiological transformation of some diterpenoids by Gibberella fijikuroi has been studied.An 18-substituent appears to exert an inhibitory effect on transformation involving reaction at the 6β-position. - Key Word Index: Gibberella fujikuroi; candol A; candol B; sideridiol; 7,18-dihydroxykaurenolide.

THE BIO-TRANSFORMATION OF SOME 6-SUBSTITUTED ENT-KAUR-16-ENES BY GIBBERELLA FUJIKUROI

Alam, Muzaffar,Hanson, James R.,Sarah, Fahmi Y.

, p. 807 - 809 (2007/10/02)

Incubation of a series of 6-oxygenated ent-kaur-16-enes with Gibberella fujikuroi affords the seco ring B derivative, fujenal, and some other metabolites.

The Acyloin Condensation of the Diterpenoid Fujenal

Hanson, James R.,Triana, Jorge

, p. 611 - 614 (2007/10/02)

The reaction of the B-seco-diterpenoid fujenal with sodium in liqiud ammonia affords two 6-monohydroxy- and two 6,7-dihydroxy-kaurenes.

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