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The chemical "3H-Cyclohepta[1,2-a:5,4-a']dinaphthalen-3-one,1,2,4,4a,5,7,7a,8,9,9a,10,11,12,13,13a,13b,14,15,15a,15b-eicosahydro-11-hydroxy-4,4,7a,10,10,13a,15b-heptamethyl-,(4aR,7aS,9aR,11S,13aR,13bS,15aS,15bR)- (9CI)" is a complex organic compound with a molecular formula of C31H38O2. It is a derivative of cyclohepta[1,2-a:5,4-a']dinaphthalen-3-one, featuring a cycloheptane ring fused to two naphthalene rings. The compound has 21 carbon atoms in its main structure, with an additional five carbon atoms in the form of methyl groups attached to various positions. It also contains a hydroxyl group at the 11th position and exhibits a specific stereochemistry, as indicated by the R and S configurations at various chiral centers. 3H-Cyclohepta[1,2-a:5,4-a']dinaphthalen-3-one,1,2,4,4a,5,7,7a,8,9,9a,10,11,12,13,13a,13b,14,15,15a,15b-eicosahydro-11-hydroxy-4,4,7a,10,10,13a,15b-heptamethyl-,(4aR,7aS,9aR,11S,13aR,13bS,15aS,15bR)- (9CI) is likely to be found in specialized chemical libraries or used in advanced organic synthesis due to its intricate structure and potential applications in material science or pharmaceutical research.

3787-73-3

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3787-73-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3787-73-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,8 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3787-73:
(6*3)+(5*7)+(4*8)+(3*7)+(2*7)+(1*3)=123
123 % 10 = 3
So 3787-73-3 is a valid CAS Registry Number.

3787-73-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3β-hydroxyserrat-14-en-21-one

1.2 Other means of identification

Product number -
Other names (4aR,7aS,9aR,11S,13aR,13bS,15aS,15bR)-11-Hydroxy-4,4,7a,10,10,13a,15b-heptamethyl-1,2,4,4a,5,7,7a,8,9,9a,10,11,12,13,13a,13b,14,15,15a,15b-icosahydro-cyclohepta[1,2-a

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:3787-73-3 SDS

3787-73-3Downstream Products

3787-73-3Relevant academic research and scientific papers

Lycopodium Triterpenoids. (12). Syntheses of Inundoside-A and -E, Triterpenoid-glycosides of Lycopodium inundatum L.

Tsuda, Yoshisuke,Haque, Md. Ekramul

, p. 1500 - 1503 (2007/10/02)

Starting from serratenediol and 21-episerratenediol, their 3-α-L-arabinopyranosides, inundoside-A and inundoside-E, triterpenoid-glycosides occurring in Lycopodium inundatum, were synthesized, thus proving their structures.Keywords---Lycopodiaceae; Lycopodium inundatum; triterpenoid-glycoside; L-arabinoside; inundoside; serratane group; Koenig-Knorr reaction

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