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75039-84-8

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75039-84-8 Usage

General Description

TRANS-2-UNDECEN-1-OL, also known as 2-Undecen-1-ol, is an organic compound with the molecular formula C11H22O. It is a colorless liquid that is used as a fragrance ingredient in cosmetic and personal care products. TRANS-2-UNDECEN-1-OL is naturally found in essential oils such as citronella and is also produced synthetically for commercial use. It has a sweet and floral odor, making it a popular choice for adding a pleasant fragrance to various consumer products. In addition to its use in fragrances, TRANS-2-UNDECEN-1-OL also has potential applications in the synthesis of other organic compounds. However, it is important to handle this chemical with care as it can be an irritant to the skin, eyes, and respiratory system.

Check Digit Verification of cas no

The CAS Registry Mumber 75039-84-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,0,3 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 75039-84:
(7*7)+(6*5)+(5*0)+(4*3)+(3*9)+(2*8)+(1*4)=138
138 % 10 = 8
So 75039-84-8 is a valid CAS Registry Number.

75039-84-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (A19698)  trans-2-Undecen-1-ol, 96%   

  • 75039-84-8

  • 5g

  • 357.0CNY

  • Detail
  • Alfa Aesar

  • (A19698)  trans-2-Undecen-1-ol, 96%   

  • 75039-84-8

  • 25g

  • 1442.0CNY

  • Detail

75039-84-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Trans-2-Undecen-1-ol

1.2 Other means of identification

Product number -
Other names TRANS-2-UNDECEN-1-OL

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:75039-84-8 SDS

75039-84-8Relevant articles and documents

Continuous Flow Z-Stereoselective Olefin Metathesis: Development and Applications in the Synthesis of Pheromones and Macrocyclic Odorant Molecules**

Browne, Duncan L.,Colombel-Rouen, Sophie,Crévisy, Christophe,Curbet, Idriss,Mauduit, Marc,McBride, Tom,Morvan, Jennifer,Roisnel, Thierry

supporting information, p. 19685 - 19690 (2021/08/06)

The first continuous flow Z-selective olefin metathesis process is reported. Key to realizing this process was the adequate choice of stereoselective catalysts combined with the design of an appropriate continuous reactor setup. The designed continuous process permits various self-, cross- and macro-ring-closing-metathesis reactions, delivering products in high selectivity and short residence times. This technique is exemplified by direct application to the preparation of a range of pheromones and macrocyclic odorant molecules and culminates in a telescoped Z-selective cross-metathesis/ Dieckmann cyclisation sequence to access (Z)-Civetone, incorporating a serial array of continually stirred tank reactors.

Zinc-catalyzed chemoselective reduction of esters to alcohols

Das, Shoubhik,Moeller, Konstanze,Junge, Kathrin,Beller, Matthias

experimental part, p. 7414 - 7417 (2011/08/05)

Economical alcohols! A general and chemoselective catalytic reduction of esters to alcohols using inexpensive zinc acetate and silanes has been developed. The operational simplicity and the high functional group tolerance, without the need for protecting and deprotecting steps, make this procedure particularly attractive for organic synthesis. Copyright

ARYL ALIPHATIC ACIDS

-

, (2008/06/13)

Novel aryl aliphatic acids or derivatives thereof of the general formula R-(Cx-Cy)-(CmH2m)-G-C(R1)2-Ar-(CnH2n)-COOR2 are described which exhibit inhibiting activity against 12-lipoxygenase. The compounds are characterized by having a low level of toxicity. Also included are salts and esters of the aliphatic acids

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