3777-71-7 Usage
Description
2-N-Heptylfuran is an organic compound with a unique chemical structure that features a furan ring and a heptyl side chain. It is known for its distinct coffee-like, nutty odor and is characterized by its taste threshold values, which include a fatty, vegetative, lactonic, herbal, and oily profile with a tropical nuance.
Uses
Used in Flavor and Fragrance Industry:
2-N-Heptylfuran is used as a flavoring agent for its unique taste characteristics, which include a combination of fatty, vegetative, lactonic, herbal, and oily notes with a tropical nuance. This makes it suitable for enhancing the flavor profiles of various food products.
2-N-Heptylfuran is also used as a fragrance ingredient due to its coffee-like, nutty odor. It can be incorporated into perfumes, colognes, and other scented products to provide a rich and complex aroma.
Used in Pharmaceutical Applications:
2-N-Heptylfuran is used as an inhibitor of BP-induced tumorigenesis in mice, indicating its potential application in the development of cancer treatments and therapies.
Used in Food Industry:
2-N-Heptylfuran is found in various cooked and heated food products, such as beef, beef fat, French fried potatoes, cooked chicken, and roasted flberts. It contributes to the overall flavor and aroma of these dishes, making it an important component in the culinary world.
Check Digit Verification of cas no
The CAS Registry Mumber 3777-71-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,7 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3777-71:
(6*3)+(5*7)+(4*7)+(3*7)+(2*7)+(1*1)=117
117 % 10 = 7
So 3777-71-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H18O/c1-2-3-4-5-6-8-11-9-7-10-12-11/h7,9-10H,2-6,8H2,1H3
3777-71-7Relevant articles and documents
Nickel-catalyzed cross-coupling of non-activated and functionalized alkyl halides with alkyl grignard reagents
Vechorkin, Oleg,Hu, Xile
supporting information; experimental part, p. 2937 - 2940 (2009/09/08)
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Substituted phthalocyanines
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, (2008/06/13)
Phthalocyanine of formula (I), wherein M is a metal or is 2H, bonded at 29 and 31 positions shown, R1 to R8 are the same or different and are independently selected from C1 to C20 alkyl, C1 -C20 alkenyl, --X--COO--X1, --X--O--Y, a, and --X--COZ where X is independently selected from a chemical bond, (CH2)n where n-0-20 or (CH2)a CH--CH (CH2)b where a and b are independently selected from 0-20 and a+b is in the range 0-20, X1 is independently selected from C1 -C20 alkyl or C2 -C20 alkenyl, Y is independently selected from C1 -C20 alkyl, C2 -C20 alkenyl or H and Z is selected from OH or NR1 R11 are independently selected from H, C1 -C20 alkyl and C2 -C20 alkenyl. These phthalocyanines may exhibit discotic liquid crystal phases, absorb infra-red radiation and make good Langmuir-Blodgett films.
CHEMISTRY OF SYSTEMS OF THE ALLYLIC TYPE II. ACYLATION OF 3-BROMO- AND 2-METHYL-3-CHLORO-1-PROPENES
Ibragimov, I. I.,Mamedov, E. I.,Ismailov, A. T.,Aliev, A. G.,Mekhtieva, Sh. Z.,et al.
, p. 1425 - 1430 (2007/10/02)
The acylation of 3-bromo- and 2-methyl-3-chloro-1-propenes under the conditions of the Kondakov-Krapivin reaction showed that the addition of acyl chlorides to these compounds takes place according to the Markovnikov rule with formation of the corresponding halogen-containing α-β-unsaturated ketones and alkyl(cycloalkyl)furans.
