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Undecanedioic acid, also known as undecyl formate, is a colorless liquid organic compound with the chemical formula C11H20O2. It is an ester derived from undecyl alcohol and formic acid, featuring a long hydrocarbon chain with an ester functional group at one end. undecyl formate is widely used in the fragrance industry as a fixative and scent enhancer, providing a musky, floral, and fruity odor profile. It is also employed as a solvent and a component in various industrial applications, such as in the production of resins, adhesives, and coatings. Due to its low toxicity and biodegradability, undecyl formate is considered a relatively safe chemical for use in consumer products.

5454-24-0

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5454-24-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5454-24-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5454-24:
(6*5)+(5*4)+(4*5)+(3*4)+(2*2)+(1*4)=90
90 % 10 = 0
So 5454-24-0 is a valid CAS Registry Number.

5454-24-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name undecyl formate

1.2 Other means of identification

Product number -
Other names 1-Undecanol,formate

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:5454-24-0 SDS

5454-24-0Downstream Products

5454-24-0Relevant academic research and scientific papers

Ir-catalyzed tandem hydroformylation-transfer hydrogenation of olefins with (trans-/cis-)formic acid as hydrogen source in presence of 1,10-phenanthroline

Chen, Xiao-Chao,Gao, Han,Liu, Lei,Liu, Ye,Lu, Yong,Xia, Fei,Yang, Shu-Qing

, p. 183 - 193 (2020/04/08)

The one-pot tandem hydroformylation-reduction to synthesize alcohols from olefins is in great demand but suffering from low yields, poor selectivity and harsh condition. Herein, 1,10-phenanthroline (L1) modified Ir-catalyst proved to exhibit multiple cata

SALT OF ISOLATED COMPOUND CONTAINING AMIDE GROUP, METHOD FOR PRODUCING THE SAME, AND METHOD FOR SYNTHESIZING AMIDE COMPOUND USING THE SAME

-

Paragraph 0105; 0107; 0115, (2018/08/23)

PROBLEM TO BE SOLVED: To provide a salt of an isolated compound containing an amide group, a method for producing the same, and a method for synthesizing an amide compound using the same. SOLUTION: The present invention provides a salt of an isolated compound containing an amide group represented by formula (1) (M is an element belonging to group 1 in the periodic table; P is a first protective group of an amine represented by R1-O(C=O)-; Q is a second protective group of an amine represented by R2-(C=O)-; R1 and R2 independently represent a substituted/unsubstituted hydrocarbon group). SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT

High-yielding tandem hydroformylation/hydrogenation of a terminal olefin to produce a linear alcohol using a Rh/Ru dual catalyst system

Takahashi, Kohei,Yamashita, Makoto,Ichihara, Takeo,Nakano, Koji,Nozaki, Kyoko

supporting information; experimental part, p. 4488 - 4490 (2010/08/19)

(Chemical equation presented) A dual catalyst system has been developed for tandem hydroformylation/hydrogenation to produce n-undecanol from 1-decene in one pot. A combination of xantphos/[Rh(acac)(CO)2] and Shvo's catalyst (1) afforded the best results (see scheme; acac = acetylacetonate, DMA = N,N-dimethylacetamide). Polar solvents effectively suppressed the formation of undecyl formate.

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