91758-26-8 Usage
Chemical structure
A cyclohexene carboxylic acid with a methyl ester, hydroxy groups, and a dimethylsilyl oxy group.
Stereochemistry
The compound has the R configuration on the third, fourth, and fifth carbon atoms.
Potential applications
Pharmaceutical or other industries due to its unique structure and properties.
Functional groups
Carboxylic acid, ester, hydroxy, and dimethylsilyl ether groups.
Molecular weight
310.45 g/mol
Physical state
Likely a solid at room temperature
Solubility
Soluble in organic solvents such as ethanol, methanol, and acetone.
Stability
Stable under normal conditions, but sensitive to heat, light, and moisture.
Reactivity
May react with strong acids, bases, or nucleophiles due to the presence of the ester and hydroxy groups.
Check Digit Verification of cas no
The CAS Registry Mumber 91758-26-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,7,5 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 91758-26:
(7*9)+(6*1)+(5*7)+(4*5)+(3*8)+(2*2)+(1*6)=158
158 % 10 = 8
So 91758-26-8 is a valid CAS Registry Number.
91758-26-8Relevant articles and documents
Studies directed towards the biosynthesis of the C7N unit of rifamycin B: A new synthesis of quinic acid from shikimic acid
Meier,Tamm
, p. 807 - 818 (2007/10/02)
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Chemistry of shikimic acid derivatives. Synthesis of specyfically labeled shikimic acid at C-3 or C-4
Zamir, Lolita O.,Luthe, Corinne
, p. 1169 - 1175 (2007/10/02)
Specifically labeled shikimic acids with tritium or deuterium at posiions C-3 or C-4 were synthesized.Commercially available L-shikimic acid was converted to its 3- and 4-ketones, after suitable protection of the hydroxyl groups at C-4, C-5 and C-3, C-5.Reduction of the 3-keto or 4-keto-shikimic acid derivatives with sodium borodeuteride and deprotection gave mostly 3-D-epi-shikimic acid or 4-D-shikimic acid.An internally assisted inversion of the 3-D-epi-shikimic acid derivative and deprotection gave 3-D-shikimic acid.
