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6917-35-7

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6917-35-7 Usage

Chemical Properties

White crystals; odorless; sweet taste. Soluble in water; insoluble in absolute alcohol and ether. Stable to heat, strong acid, and alkali. Amounts are expressed in milligrams of inositol.

Uses

Different sources of media describe the Uses of 6917-35-7 differently. You can refer to the following data:
1. Cyclohexane-1,2,3,4,5,6-hexol is used in emollients for its ability to hold and retain moisture, it belongs to the vitamin B family. Although found naturally in plant and animal tissue, for commercial use it is isolated from corn.
2. Inositol is an essentially non toxic compound largely formed by the dephosphorylation of inositol hexaphosphate (IP6, Phytate) with in the gastrointestinal tract in humans and animals.
3. Medicine, nutrition, intermediate.

Definition

Cyclohexane-1,2,3,4,5,6-hexol is a constituent of body tissue. There are nine isomeric forms of inositol (myo-inositol or mesoinositol or specifically the cis-1,2,3,5-trans-4,6- hexahydroxycyclohexane has vitamin activity).

Check Digit Verification of cas no

The CAS Registry Mumber 6917-35-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,1 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6917-35:
(6*6)+(5*9)+(4*1)+(3*7)+(2*3)+(1*5)=117
117 % 10 = 7
So 6917-35-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O6/c7-1-2(8)4(10)6(12)5(11)3(1)9/h1-12H/t1-,2-,3-,4+,5-,6-

6917-35-7SDS

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 Cyclohexane-1,2,3,4,5,6-Hexol

1.2 Other means of identification

Product number -
Other names 1,2,3,4,5,6-Cyclohexanehexol

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:6917-35-7 SDS

6917-35-7Relevant articles and documents

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.

Optically active phenoxypropionic esters

-

, (2008/06/13)

Optically active compounds of the formula I STR1 where R is C1 -C12 -alkyl or -perfluoroalkyl in which one or two non-adjacent CH2 or CF2 groups can also be replaced by --O-- and/or --CO-- and/or --CO--O-- and/or --CH=CH-- and/or --CH-halogen-- and/or --CHCN-- and/or --0--CO--CH-halogen-- and/or --O--CO--CHCN--, or is C1 -C12 -alkyl which can have a terminal chemically reactive group and in which a CH2 group can be replaced by --O--, A1 and A2 are each, independently of one another, 1,4-phenylene which is unsubstituted or substituted by one or two F and/or Cl and/or Br atoms and/or CH3 groups and/or CN groups and in which one or two CH groups can also be replaced by N, 1,4-cyclohexylene in which one or two non-adjacent CH2 groups can also be replaced by --O-- and/or --S--, 1,4-piperidinediyl, 1,4-bicyclo[2.2.2]octylene, 2,6-naphthalenediyl, decahydro-2,6-naphthalenediyl or 1,2,3,4-tetrahydro-2,6-naphthalenediyl, A3 is unsubstituted or substituted phenyl, Z is --CO--O--, --O--CO--, --CH2 CH2 --, --OCH2 --, --CH2 O--, --C C-- or a single bond and m is 0, 1, 2 or 3.

Unusual Oxidation of 1-Halo-1,3-dienes with Permanganate. Expedient Syntheses of (+)-D-chiro-3-Inosose and (+)-D-chiro-Inositol from Chlorobenzene

Mandel, Martin,Hudlicky, Tomas,Kwart, Lawrence D.,Whited, Gregg M.

, p. 2331 - 2333 (2007/10/02)

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