D-myo-Inositol, 2,5,6-tris-O-(phenylmethyl)-3,4-O-(1R,2S,4R)-1,7,7-trimethylbicyclo2.2.1hept-2-ylidene-

Base Information

Chemical Name:D-myo-Inositol, 2,5,6-tris-O-(phenylmethyl)-3,4-O-(1R,2S,4R)-1,7,7-trimethylbicyclo2.2.1hept-2-ylidene-
CAS No.:226889-37-8
Molecular Formula:C₃₇H₄₄O₆
Molecular Weight:584.753
Hs Code.:

Synonyms:D-myo-Inositol, 2,5,6-tris-O-(phenylmethyl)-3,4-O-(1R,2S,4R)-1,7,7-trimethylbicyclo2.2.1hept-2-ylidene-

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Chemical Property of D-myo-Inositol, 2,5,6-tris-O-(phenylmethyl)-3,4-O-(1R,2S,4R)-1,7,7-trimethylbicyclo2.2.1hept-2-ylidene-

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Technology Process of D-myo-Inositol, 2,5,6-tris-O-(phenylmethyl)-3,4-O-(1R,2S,4R)-1,7,7-trimethylbicyclo2.2.1hept-2-ylidene-

There total 56 articles about D-myo-Inositol, 2,5,6-tris-O-(phenylmethyl)-3,4-O-(1R,2S,4R)-1,7,7-trimethylbicyclo2.2.1hept-2-ylidene- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 31.0%

: 109280-15-1
(1R)-(+)-camphor dimethyl acetal

: 98906-30-0,104873-76-9,111466-07-0,114297-88-0,114297-91-5,114419-08-8,115184-71-9,115509-75-6,115509-76-7,118354-54-4,118354-55-5,128163-34-8,129706-80-5,136521-84-1,149713-88-2,149713-95-1
(+/-)-2,5,6-tri-O-benzyl-myo-inositol

: 196306-65-7,226889-35-6,226889-37-8,226889-38-9
C₃₇H₄₄O₆

: 196306-65-7,226889-35-6,226889-37-8,226889-38-9
C₃₇H₄₄O₆

: 196302-88-2,196306-65-7,226889-35-6,226889-37-8,226889-38-9
1D-2,4,5-tri-O-benzyl-1-O-endo,6-O-exo-(D-1',7',7'-trimethylbicyclo<2.2.1>hept-2'-ylidene)-myo-inositol

Guidance literature:: With toluene-4-sulfonic acid; In dichloromethane; Title compound not separated from byproducts; Heating;
DOI:10.1039/a703044d

Reference yield: 31.0%

: 109280-15-1
(1R)-(+)-camphor dimethyl acetal

: 98906-30-0,104873-76-9,111466-07-0,114297-88-0,114297-91-5,114419-08-8,115184-71-9,115509-75-6,115509-76-7,118354-54-4,118354-55-5,128163-34-8,129706-80-5,136521-84-1,149713-88-2,149713-95-1
(+/-)-2,5,6-tri-O-benzyl-myo-inositol

: 196306-65-7,226889-35-6,226889-37-8,226889-38-9
C₃₇H₄₄O₆

: 196306-65-7,226889-35-6,226889-37-8,226889-38-9
C₃₇H₄₄O₆

: 196302-88-2,196306-65-7,226889-35-6,226889-37-8,226889-38-9
1D-2,4,5-tri-O-benzyl-1-O-endo,6-O-exo-(D-1',7',7'-trimethylbicyclo<2.2.1>hept-2'-ylidene)-myo-inositol

Guidance literature:: With toluene-4-sulfonic acid; In dichloromethane; Title compound not separated from byproducts; Heating;
DOI:10.1039/a703044d

Reference yield: 31.0%

: 109280-15-1
(1R)-(+)-camphor dimethyl acetal

: 98906-30-0,104873-76-9,111466-07-0,114297-88-0,114297-91-5,114419-08-8,115184-71-9,115509-75-6,115509-76-7,118354-54-4,118354-55-5,128163-34-8,129706-80-5,136521-84-1,149713-88-2,149713-95-1
(+/-)-2,5,6-tri-O-benzyl-myo-inositol

: 196306-65-7,226889-35-6,226889-37-8,226889-38-9
C₃₇H₄₄O₆

: 196306-65-7,226889-35-6,226889-37-8,226889-38-9
C₃₇H₄₄O₆

: 196302-88-2,196306-65-7,226889-35-6,226889-37-8,226889-38-9
1D-2,4,5-tri-O-benzyl-1-O-endo,6-O-exo-(D-1',7',7'-trimethylbicyclo<2.2.1>hept-2'-ylidene)-myo-inositol

Guidance literature:: With toluene-4-sulfonic acid; In dichloromethane; Title compound not separated from byproducts; Heating;
DOI:10.1039/a703044d