PRODUCT IDENTIFICATION
CLASSIFICATION
PHYSICAL AND CHEMICAL PROPERTIES
REFRACTIVE INDEX
GENERAL DESCRIPTION & APPLICATIONS
APPEARANCE
98.0% min
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| METHYL CYCLOPENTYLPHENYLGLYCOLATE | ||
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PRODUCT IDENTIFICATION |
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| CAS NO. | 19833-96-6 |
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| EINECS NO. | 243-359-0 | |
| FORMULA | C5H4C(OH)(C6H11)COOCH3 | |
| MOL WT. | 234.29 | |
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| SYNONYMS | Cyclopentylphénylglycolate de méthyle; | |
| alpha-Cyclopentylmandelic acid methyl ester; alpha-Cyclopentyl mandelic acid methyl ester; Cyclopentyl-hydroxy-phenyl-acetate; Methylcyclopentylphenylglykolat; Ciclopentilfenilglicolato de metilo; | ||
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CLASSIFICATION |
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PHYSICAL AND CHEMICAL PROPERTIES |
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| PHYSICAL STATE | white to yellow crystalline powder | |
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| NFPA RATINGS | Health: 3; Flammability: 0; Instability: 0 | |
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REFRACTIVE INDEX |
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| FLASH POINT | ||
| STABILITY | Stable under ordinary conditions. | |
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GENERAL DESCRIPTION & APPLICATIONS |
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| The Grignard Reaction is the organometallic halide (mainly alkyl- or aryl- magnesium halides) addition to a ketone or acid chlorides to form a tertiary alcohol. The reaction with formaldehyde and aldehyde yields a primary alcohol and secondary alcohol respectively. It is unreasonable to expect oxidation reaction of tertiary alcohols which don't have a hydrogen atom attached to alpha carbon. Tertiary alcohol can yield alkenes (dehydration reaction) and alkyl halide (SN1 reaction) in the presence of acid catalyst. Cyclopentylphenylglycolic acid is a tertiary alcohol which benzene, cyclopentane and acetic acid are attached to alpha carbon. This compound is an alpha-hydroxy acid which has a hydroxyl group on the carbon atom next to the acid group. In structure this compound belong to mandelic acid. This structure is a moiety of glycopyrrolate (CAS RN: 596-51-0) which is a muscarinic antagonist used as an antispasmodic, in some disorders of the gastrointestinal tract, and to reduce salivation with some anesthetics. | ||
| SALES SPECIFICATION | ||
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APPEARANCE |
white to yellow crystalline powder | |
| ASSAY |
98.0% min |
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