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OH-chlorobactene is a naturally occurring chemical compound found in certain bacteria, particularly in the genus Pseudomonas. It is a secondary metabolite, which means it is not essential for the bacteria's growth but may play a role in their survival or interaction with the environment. OH-chlorobactene is characterized by its unique structure, which includes a chlorinated polycyclic aromatic hydrocarbon with a hydroxyl group attached. OH-chlorobactene has been studied for its potential antimicrobial properties and its ability to inhibit the growth of other microorganisms. Research on OH-chlorobactene and related compounds is ongoing, as scientists explore their potential applications in medicine and biotechnology, such as in the development of new antibiotics or as tools for understanding bacterial communication and behavior.

2932-10-7

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2932-10-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2932-10-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,3 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2932-10:
(6*2)+(5*9)+(4*3)+(3*2)+(2*1)+(1*0)=77
77 % 10 = 7
So 2932-10-7 is a valid CAS Registry Number.

2932-10-7Downstream Products

2932-10-7Relevant academic research and scientific papers

Carotenoid Sulfates. 4. Syntheses and Properties of Carotenoid Sulfates

Hertzberg, Sissel,Liaaen-Jensen, Synnoeve

, p. 629 - 638 (2007/10/02)

Carotenoid sulfates have been prepared from 14 selected carotenols for spectroscopic characterization, studies of their stability in solution and their water solubility.Carotenoids containing sec non-allylic hydroxy groups provided sulfates stable in methanol solution, exemplified by zeaxanthin mono- and disulfate, alloxathin mono- and disulfate, fucoxanthin monosulfate, peridinin monosufate, capsorubin mono- and disulfate and astaxanthin mono- and disulfate.Acid catalyzed methanolysis of zeaxanthin disulfate gave zeaxanthin with complete retention of configuration.Enzymatic hydrolysis of alloxanthin monosulfate is reported.Less stable sulfates were obtained from sec vic diol type-, phenolic and tert-carotenols; caloxanthin, nostoxanthin, 3-hydroxyisorenieratene, 3,3'-dihydroxyisorenieratene, rhodovibrin, di-OH-lycopene and OH-chlorobactene.Acid catalyzed methanolysis of the tert caratenols proceeded via carbocations, judged by the solvolysis products characterized.Characteristic spectroscopic properties of carotenoid sulfates are pointed out.Water solubilities were studied.

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