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26612-48-6

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26612-48-6 Usage

General Description

Caulerpin is a natural chemical compound found in certain types of marine algae, particularly in species of Caulerpa. It is a unique molecule with a terpenoid backbone and a tetrahydrofuran ring, making it a diterpene. Caulerpin has been reported to have various biological activities, including antifungal, antibacterial, antiviral, and antitumor properties. It has also been studied for its potential use in medical applications, such as in drug development for cancer treatment. Additionally, caulperin has shown promise in research for its potential use in the development of new materials, such as adhesives and coatings, due to its ability to form strong hydrogen bonds. Overall, caulperin is a complex and intriguing compound with a wide range of potential applications in medicine and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 26612-48-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,6,1 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 26612-48:
(7*2)+(6*6)+(5*6)+(4*1)+(3*2)+(2*4)+(1*8)=106
106 % 10 = 6
So 26612-48-6 is a valid CAS Registry Number.

26612-48-6SDS

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 caulerpine

1.2 Other means of identification

Product number -
Other names caulerpin

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:26612-48-6 SDS

26612-48-6Synthetic route

methanol
67-56-1

methanol

(6E,13E)-5,12-dihydrocycloocta[1,2-b:5,6-b']diindole-6,13-dicarboxylic caulerpic acid
28056-19-1

(6E,13E)-5,12-dihydrocycloocta[1,2-b:5,6-b']diindole-6,13-dicarboxylic caulerpic acid

Caulerpin
26612-48-6

Caulerpin

Conditions
ConditionsYield
With sulfuric acid
Caulerpin
26612-48-6

Caulerpin

(6E,13E)-5,12-dihydrocycloocta[1,2-b:5,6-b']diindole-6,13-dicarboxylic caulerpic acid
28056-19-1

(6E,13E)-5,12-dihydrocycloocta[1,2-b:5,6-b']diindole-6,13-dicarboxylic caulerpic acid

Conditions
ConditionsYield
With barium dihydroxide In ethanol; water 55 deg C, 6h then r.t. overnight;21 mg
Stage #1: Caulerpin With sodium hydroxide In methanol at 50℃; for 4h;
Stage #2: With hydrogenchloride In methanol; water pH=5;

26612-48-6Relevant articles and documents

TWO CAULERPIN ANALOGUES AND A SESQUITERPENE FROM CAULERPA RACEMOSA

Anjaneyulu, A. S. R.,Prakash, C. V. S.,Mallavadhani, U. V.

, p. 3041 - 3042 (1991)

The ethyl acetate extract of Caulerpa racemosa yielded two new red pigments which are caulerpin analogues.A new sesquiterpenoid present was identified as 10-keto-3,7,11-trimethyldodecanoic acid.Key Word Index - Caulerpa racemosa; marine green alga; red pi

Simple synthesis method of caulerpin

-

Paragraph 0045; 0050, (2018/09/21)

The invention belongs to the field of organic chemical synthesis, and discloses a simple synthesis method of caulerpin. The method includes the steps of firstly, using indole as the raw material without protecting amidogen on the indole, and conducting affinity substitution of methyl acetate on a second site of the indole to generate indole-2-methyl acetate; secondly, conducting a formylation reaction on a third site of the indole-2-methyl acetate to obtain 3-formyl-2-indole methyl acetate; finally, conducting between-two-molecule cyclization on the 3-formyl-2-indole methyl acetate to obtain the caulerpin. Compared with the prior art, the method is simple in process, low in raw material cost, mild in reaction condition, beneficial for industrialization, quite high in medical value and widein market prospect, and the synthesis cycle is greatly shortened.

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