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Nonacosan-10-ol, also known as 10-hydroxynonacosane, is a long-chain alcohol with a molecular formula of C29H60O. It is a waxy, white solid that is insoluble in water but soluble in organic solvents. This chemical compound is primarily found in the cuticular wax of plants, where it plays a role in protecting the plant from environmental stressors such as water loss and pathogens. Nonacosan-10-ol is also used in the fragrance industry due to its pleasant, floral scent, and it can be found in various essential oils, such as jasmine and gardenia. Additionally, it has potential applications in the pharmaceutical and cosmetic industries due to its moisturizing and skin-conditioning properties.

504-55-2

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504-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 504-55-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 504-55:
(5*5)+(4*0)+(3*4)+(2*5)+(1*5)=52
52 % 10 = 2
So 504-55-2 is a valid CAS Registry Number.

504-55-2SDS

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 nonacosan-10-ol

1.2 Other means of identification

Product number -
Other names Ginnol

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:504-55-2 SDS

504-55-2Relevant academic research and scientific papers

Preparation of functionalized dialkylzincs via a boron-zinc exchange. Reactivity and catalytic asymmetric addition to aldehydes

Langer, Falk,Schwink, Lothar,Devasagayaraj, Arokiasamy,Chavant, Pierre-Yves,Knochel, Paul

, p. 8229 - 8243 (2007/10/03)

The hydroboration of olefins with Et2BH provides diethyl(alkyl)boranes 2 which readily undergo a boron - zinc exchange with Et2Zn providing a range of polyfunctional primary, secondary, and benzylic diorganozincs. The resulting diorganozincs 3 have been reacted with various electrophiles (allylic halides, acid chlorides, alkylidenemalonates, ethyl propiolate, nitroolefins) in the presence of CuCN·2LiCl with excellent yields. With secondary dialkylzincs prepared from diastereomerically pure diethyl(alkyl)boranes, the boron-zinc exchange occurs with loss of stereochemistry. The asymmetric addition of 3 to aldehydes in the presence of the chiral catalyst 55 furnishes optically active polyfunctional secondary alcohols (50 to over 96% ee).

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