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3-Oxatricyclo[2.2.1.02,6]heptane-1-carboxylic acid, 5-hydroxy, methyl ester, stereoisomer (9CI) is a complex organic compound with a unique molecular structure. It belongs to the class of chemicals known as tricyclo derivatives, which are characterized by their three-ring structure. This specific compound features a 3-oxatricyclo[2.2.1.02,6]heptane core, which is a seven-membered ring with one oxygen atom incorporated into the structure. The molecule also contains a 5-hydroxy group, indicating the presence of a hydroxyl (-OH) group at the 5th position, and a methyl ester group, which is a methyl (-CH3) group attached to a carboxylic acid (-COOH) group through an ester linkage. The term "stereoisomer" in the name suggests that 3-Oxatricyclo[2.2.1.02,6]heptane-1-carboxylicacid,5-hydroxy-,methylester,stereoisomer(9CI) exists in different spatial arrangements of atoms, which can affect its physical and chemical properties. 3-Oxatricyclo[2.2.1.02,6]heptane-1-carboxylicacid,5-hydroxy-,methylester,stereoisomer(9CI) is of interest in the field of organic chemistry and may have potential applications in pharmaceuticals or other industries due to its specific structural features.

90762-16-6

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90762-16-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90762-16-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,7,6 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 90762-16:
(7*9)+(6*0)+(5*7)+(4*6)+(3*2)+(2*1)+(1*6)=136
136 % 10 = 6
So 90762-16-6 is a valid CAS Registry Number.

90762-16-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-6-methoxycarbonyl-7-oxa-tricyclo<2.2.1.02,6>heptane

1.2 Other means of identification

Product number -
Other names 3-hydroxy-6-methoxycarbonyl-7-oxa-tricyclo[2.2.1.02,6]heptane

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:90762-16-6 SDS

90762-16-6Downstream Products

90762-16-6Relevant academic research and scientific papers

BRIEF SYNTHESES OF (+/-)-METHYL SHIKIMATE, (+/-)-METHYL EPISHIKIMATE AND STRUCTURAL VARIANTS

Campbell, Malcolm M.,Kaye, Aston D.,Sainsbury, Malcolm,Yavarzadeh, Roya

, p. 2461 - 2470 (2007/10/02)

Two brief syntheses of (+/-)-methyl shikimate are described in a strategy which offers potentially flexible access to a range of analogues.New intramolecular rearrangement reactions of epoxides derived from methyl 7-oxabicyclohept-3-ene 6-carboxylate and methyl bicyclohept-3-ene 6 carboxylate are described.

SHIKIMIC ACIDS FROM FURAN; METHODS OF STEREOCONTROLLED ACCESS TO 3,4,5-TRIOXIGENATED CYCLOHEXENES

Rajapaksa, D.,Keay, B. A.,Rodrigo, R.

, p. 826 - 828 (2007/10/02)

Oxabicycloheptenes 1 and 2 are converted to 3,4,5-oxigenated cyclohexenes by stereocontrolled hydroxylations and epoxidations coupled with reverse-Michael cleavage of the oxabicyclo system.Three epimers of shikimic acid are synthesized by these methods.

COMPLEMENTARY SHORT SYNTHESES OF (+/-)-METHYL SHIKIMATE

Campbell, Malcolm M.,Kaye, Aston D.,Sainsbury, Malcolm,Yavarzadeh, Roya

, p. 1629 - 1630 (2007/10/02)

Two syntheses of (+/-)-methyl shikimate from the adduct of furan and methyl acrylate are described.One requires the regioselective hydroxylation of (+/-)-5β,6β-dihydroxy-O,O-isopropylidene-2-methoxycarbonylcyclohexa-1,3-diene and the other cis-dihydroxyla

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