551-72-4 Usage
Description
L-(-)-CHIRO-INOSITOL, also known as L-(-)-1,2,3,5/4,6-cyclohexanehexol, is a naturally occurring optically active form of inositol, a sugar alcohol belonging to the polyol family. It is a white crystalline powder with unique chemical properties that make it a versatile compound in various applications.
Uses
Used in Pharmaceutical Research:
L-(-)-CHIRO-INOSITOL is used as a research compound for its potential role in modulating amyloid-β aggregation, which is associated with neurodegenerative diseases such as Alzheimer's.
Used in Diabetes Research:
L-(-)-CHIRO-INOSITOL is used as a research compound for its in vitro insulin-like effect and its ability to enhance glucose uptake in muscle cells. This is achieved through the induced translocation of glucose transporter 4, which is crucial for maintaining proper glucose homeostasis and managing diabetes.
Used in Chemical Synthesis:
L-(-)-CHIRO-INOSITOL, due to its unique chemical structure, is used as a building block or intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Nutritional Supplements:
L-(-)-CHIRO-INOSITOL is used as an ingredient in nutritional supplements, particularly those aimed at supporting insulin sensitivity and glucose metabolism.
Used in Food Industry:
L-(-)-CHIRO-INOSITOL may be used in the food industry as a natural sweetener or as an additive to improve the texture and stability of certain products.
Used in Cosmetics:
L-(-)-CHIRO-INOSITOL could be utilized in the cosmetics industry for its potential skin health benefits, such as improving skin hydration and elasticity.
Check Digit Verification of cas no
The CAS Registry Mumber 551-72-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,5 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 551-72:
(5*5)+(4*5)+(3*1)+(2*7)+(1*2)=64
64 % 10 = 4
So 551-72-4 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+/m1/s1
551-72-4Relevant 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
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, (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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