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2-N-Octylcyclopropanecarboxylic acid is a carboxylic acid derivative with the molecular formula C14H26O2. It features a cyclopropane ring and an octyl chain, making it a versatile chemical compound for various applications.

15898-87-0

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15898-87-0 Usage

Uses

Used in Pharmaceutical Industry:
2-N-Octylcyclopropanecarboxylic acid is used as an intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into complex molecular structures, potentially enhancing the properties and effectiveness of certain drugs.
Used in Agrochemical Industry:
In the agrochemical sector, 2-N-Octylcyclopropanecarboxylic acid serves as a building block for the development of new agrochemicals, such as pesticides and herbicides, due to its unique chemical structure that can be tailored for specific agricultural applications.
Used in Organic Synthesis:
2-N-Octylcyclopropanecarboxylic acid is used as a starting material in the synthesis of other organic compounds, allowing for the creation of new molecules with targeted properties for various industries.
Used in Material Science:
Due to its unique chemical structure, 2-N-Octylcyclopropanecarboxylic acid may be utilized in material science for the development of new materials with specific characteristics, such as improved stability or reactivity.
Used in Biomedical Research:
2-N-Octylcyclopropanecarboxylic acid may have potential applications in biomedical research, where its chemical properties could be leveraged for the advancement of diagnostic tools, therapeutic agents, or other medical innovations.

Check Digit Verification of cas no

The CAS Registry Mumber 15898-87-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,9 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15898-87:
(7*1)+(6*5)+(5*8)+(4*9)+(3*8)+(2*8)+(1*7)=160
160 % 10 = 0
So 15898-87-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H22O2/c1-2-3-4-5-6-7-8-10-9-11(10)12(13)14/h10-11H,2-9H2,1H3,(H,13,14)

15898-87-0SDS

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 2-octylcyclopropane-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-Octyl-cyclopropancarbonsaeure

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:15898-87-0 SDS

15898-87-0Downstream Products

15898-87-0Relevant academic research and scientific papers

The (+)-cis- and (+)-trans-Olibanic Acids: Key Odorants of Frankincense

Cerutti-Delasalle, Céline,Mehiri, Mohamed,Cagliero, Cecilia,Rubiolo, Patrizia,Bicchi, Carlo,Meierhenrich, Uwe J.,Baldovini, Nicolas

, p. 13719 - 13723 (2016/10/26)

Frankincense (olibanum) is one of the oldest aromatic materials used by humans, but the key molecular constituents contributing to its characteristic odor remained unknown. Reported herein is the discovery that (1S,2S)-(+)-trans- and (1S,2R)-(+)-cis-2-octylcyclopropyl-1-carboxylic acids are highly potent and substantive odorants occurring in ppm amounts in all of the frankincense samples analyzed, even those showing radically different volatile compositions. These cyclopropyl-derived acids provide the very characteristic old churchlike endnote of the frankincense odor.

Acyl and carbamimidoyl alkanediamines

-

, (2008/06/13)

Synthetically produced substantially pure biologically active compounds having the general formula STR1 wherein R1 is C1 -C20 alkyl, alkenyl, aryl, aralkyl, cycloalkyl, alkylcycloalkyl, cycloalkylalkyl, cycloalkenyl, alkylcycloalkenyl, or cycloalkenylalkyl; R2 is hydrogen, C1 -C10 alkyl or an amide-substituted alkyl having up to 10 carbon atoms; R3 is a cyclic, straight or branched chain hydrocarbon group having 2-12 carbon atoms, particularly --(CH2)n --, wherein n is 2-12; or R2 and R3 are linked together to form an alkylene chain; and R4 is selected from STR2 (substituted or unsubstituted carbamimidoyl), STR3 (dimethylpyrimidyl), or STR4 (carbamyl) wherein each of R5, R6, and R7 is hydrogen or the same or different C1 -C8 alkyl group. The compounds are useful as bactericides for a wide variety of bacteria, including S.pyogenes, B.subtilis, K.pneumoniae, M.avium, B.fragilis, C.perfringens and C.albicans.

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