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2-carboxy-1-isopropylcyclopropylmethanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

702-89-6

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702-89-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 702-89-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 702-89:
(5*7)+(4*0)+(3*2)+(2*8)+(1*9)=66
66 % 10 = 6
So 702-89-6 is a valid CAS Registry Number.

702-89-6Relevant academic research and scientific papers

Carboxylic acids in secondary aerosols from oxidation of cyclic monoterpenes by ozone

Glasius, Marianne,Lahaniati, Maria,Calogirou, Aggelos,Di Bella, Dario,Jensen, Niels R.,Hjorth, Jens,Kotzias, Dimitrios,Larsen, Bo R.

, p. 1001 - 1010 (2000)

A series of smog chamber experiments have been conducted in which five cyclic monoterpenes were oxidized by ozone. The evolved secondary aerosol was analyzed by GC-MS and HPLC-MS for nonvolatile polar oxidation products with emphasis on the identification of carboxylic acids. Three classes of compounds were determined at concentration levels corresponding to low percentage molar yields: i.e. dicarboxylic acids, oxocarboxylic acids, and hydroxyketocarboxylic acids. Carboxylic acids are highly polar and have lower vapor pressures than their corresponding aldehydes and may thus play an important role in secondary organic aerosol formation processes. The most abundant carboxylic acids were the following: cis-pinic acid AB1 (cis-3- carboxy-2,2-dimethylcyclobutylethanoic acid) from α-and β-pinene; cis- pinonic acid A3 (cis-3-acetyl-2,2-dimethylcyclobutylethanoic acid) and cis- 10-hydroxypinonic acid AB6 (cis-2,2-dimethyl-3- hydroxyacetylcyclobutylethanoic acid) from α-pinene and β-pinene; cis-3- caric acid C1 (cis-2,2-dimethyl-1,3-cyclopropyldiethanoic acid), cis-3- caronic acid C3 (2,2-dimethyl-3-(2-oxopropyl)cyclopropanylethanoic acid), and cis-10-hydroxy-3-caronic acid C6 (cis-2,2-dimethyl-3-(hydroxy-2- oxopropyl)cyclopropanylethanoic acid) from 3-carene; cis-sabinic acid S1 (cis-2-carboxy-1-isopropylcyclopropylethanoic acid) from sabinene; limonic acid L1 (3-isopropenylhexanedioic acid), limononic acid L3 (3-isopropenyl-6- oxo-heptanoic acid), 7-hydroxylimononic acid L6 (3-isopropenyl-7-hydroxy-6- oxoheptanoic acid), and 7-hydroxylimononic acid L6' (7-hydroxy-3-isopropenyl- 6-oxoheptanoic acid) from limonene. A series of smog chamber experiments have been conducted in which five cyclic monoterpenes were oxidized by ozone. The evolved secondary aerosol was analyzed by GC-MS and HPLC-MS for nonvolatile polar oxidation products with emphasis on the identification of carboxylic acids. Three classes of compounds were determined at concentration levels corresponding to low percentage molar yields: i.e. dicarboxylic acids, oxocarboxylic acids, and hydroxyketocarboxylic acids. Carboxylic acids are highly polar and have lower vapor pressures than their corresponding aldehydes and may thus play an important role in secondary organic aerosol formation processes. The most abundant carboxylic acids were the following: cis-pinic acid AB1 (cis-3-carboxy-2,2-dimethylcyclobutylethanoic acid) from α- and β-pinene; cis-pinonic acid A3 (cis-3-acetyl-2,2-dimethylcyclobutylethanoic acid) and cis-10-hydroxypinonic acid AB6 (cis-2,2-dimethyl-3-hydroxyacetylcyclobutyl-ethanoic acid) from α-pinene and β-pinene; cis-3-caric acid C1 (cis-2,2-dimethyl-1,3-cyclopropyldiethanoic acid), cis-3-caronic acid C3 (2,2-dimethyl-3-(2-oxopropyl)cyclopropanylethanoic acid), and cis-10-hydroxy-3-caronic acid C6 (cis-2,2-dimethyl-3-(hydroxy-2-oxopropyl)cyclopropanyl-ethanoic acid) from 3-carene; cis-sabinic acid S1 (cis-2-carboxy-1-isopropylcyclopropylethanoic acid) from sabinene; limonic acid L1 (3-isopropenylhexanedioic acid), limononic acid L3 (3-isopropenyl-6-oxo-heptanoic acid), 7-hydroxy-limononic acid L6 (3-isopropenyl-7-hydroxy-6-oxoheptanoic acid), and 7-hydroxylimononic acid L6′ (7-hydroxy-3-isopropenyl-6-oxoheptanoic acid) from limonene.

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