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Myo-inositol hexabenzoate is a chemical compound derived from myo-inositol, a naturally occurring sugar alcohol, and benzoic acid. It is formed by the esterification of myo-inositol with six benzoic acid molecules, resulting in a complex ester. myo-Inositol hexabenzoate is known for its potential applications in various fields, including pharmaceuticals, as a stabilizer or solubility enhancer for certain drugs, and in the chemical industry for its unique properties. Myo-inositol hexabenzoate is also of interest in research due to its ability to influence certain biological processes, although its specific uses and effects are subject to ongoing study.

4099-90-5

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4099-90-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4099-90-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,9 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4099-90:
(6*4)+(5*0)+(4*9)+(3*9)+(2*9)+(1*0)=105
105 % 10 = 5
So 4099-90-5 is a valid CAS Registry Number.
InChI:InChI=1/C48H36O12/c49-43(31-19-7-1-8-20-31)55-37-38(56-44(50)32-21-9-2-10-22-32)40(58-46(52)34-25-13-4-14-26-34)42(60-48(54)36-29-17-6-18-30-36)41(59-47(53)35-27-15-5-16-28-35)39(37)57-45(51)33-23-11-3-12-24-33/h1-30,37-42H

4099-90-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,3,4,5,6-pentabenzoyloxycyclohexyl) benzoate

1.2 Other means of identification

Product number -
Other names hexa-O-benzoyl-myo-inositol

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:4099-90-5 SDS

4099-90-5Downstream Products

4099-90-5Relevant academic research and scientific papers

Carbohydrates from Detarium microcarpum bark extract

Abreu, Pedro,Relva, Angela

, p. 1663 - 1666 (2002)

The bark extract of the medicinal plant Detarium microcarpum was analysed for its carbohydrate content by GLC-CIMS. Preparative HPLC of the benzoylated carbohydrate fraction led to the isolation of L-quino-1,5-lactone, D-(-)-bornesitol, D-pinitol, myo-ino

Transformation of cyclohexene to enantiopure cyclitols mediated by sequential oxyselenenylation with (S,S)-hydrobenzoin: Synthesis of D-chiro-inositol and muco-quercitol

Kim, Kwan Soo,Park, Jong H.,Moon, Hoi Kyung,Yi, Hann

, p. 1945 - 1946 (2007/10/03)

Oxyselenenylation of cyclohexene with (S,S)-hydrobenzoin and subsequent oxidation-elimination allows isolation of an allylic ether in which further phenylselenenylation is completely regioselective, thus allowing entry to the cyclitols D-chiro-inositol and muco-quercitol.

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