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2-(2-FURYL)-2-HEXANOL, also known as 2-(2-furyl)hexan-2-ol or CAS number 5989-27-7, is an organic compound characterized by a hexanol backbone with a furyl group attached to the second carbon. This molecule consists of a six-carbon chain with a hydroxyl group at the second position and a furyl ring (a five-membered aromatic ring with four carbons and one oxygen) at the same position. It is a colorless to pale yellow liquid with a distinct odor and is soluble in organic solvents. This chemical is primarily used as a fragrance ingredient in various consumer products, such as perfumes, cosmetics, and detergents, due to its unique scent profile. It is also employed as a synthetic intermediate in the production of other chemicals. However, it is essential to handle 2-(2-furyl)-2-hexanol with care, as it may cause skin and eye irritation, and prolonged exposure may have adverse health effects.

6137-76-4

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6137-76-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6137-76-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,3 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6137-76:
(6*6)+(5*1)+(4*3)+(3*7)+(2*7)+(1*6)=94
94 % 10 = 4
So 6137-76-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O2/c1-3-4-7-10(2,11)9-6-5-8-12-9/h5-6,8,11H,3-4,7H2,1-2H3

6137-76-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-Furyl)-2-hexanol

1.2 Other means of identification

Product number -
Other names Methyl-(1-butyl)-(2-furyl)carbinol

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:6137-76-4 SDS

6137-76-4Relevant academic research and scientific papers

Efficient chemoselective addition of grignard reagents to carbonyl compounds in 2-methyltetrahydrofuran

Zhong, Weihui,Wu, Yaotiao,Zhang, Xingxian

experimental part, p. 370 - 373 (2009/12/25)

Compared with tetrahydrofuran (THF) as a solvent for the addition reactions between Grignard reagents and carbonyl compounds 2-methyltetrahydrofuran affords the corresponding adducts in higher yields with higher chemoselectivities. Moreover, 2-methyltetrahydrofuran can be readily recycled and reused, which lowers the cost of the process and makes the reaction greener.

A general sultone route to the pamamycin macrodiolides - Total synthesis of pamamycin-621A and pamamycin-635B

Fischer, Petra,Segovia, Ana Belen Garcia,Gruner, Margit,Metz, Peter

, p. 6231 - 6234 (2007/10/03)

(Chemical Equation Presented) Sultones swing again: The first total syntheses of the title antibiotics (see scheme) were achieved by application of sultone methodology. Since the final lactonizations with formation of the ester linkage between C1′ and the

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