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70419-06-6

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70419-06-6 Usage

Uses

(S)-(+)-2-Nonanol can be used as a reactant to prepare: Nonan-2-yl 4-nitrobenzoate by reacting with 4-nitrobenzoic acid in Mitsunobu reaction conditions. Chiral conjugated polythiophene derivatives from achiral monomers in nematic liquid crystal solvent.

Check Digit Verification of cas no

The CAS Registry Mumber 70419-06-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,4,1 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 70419-06:
(7*7)+(6*0)+(5*4)+(4*1)+(3*9)+(2*0)+(1*6)=106
106 % 10 = 6
So 70419-06-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H20O/c1-3-4-5-6-7-8-9(2)10/h9-10H,3-8H2,1-2H3/t9-/m0/s1

70419-06-6 Well-known Company Product Price

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  • Aldrich

  • (557978)  (S)-(+)-2-Nonanol  97%, optical purity98%

  • 70419-06-6

  • 557978-1G

  • 1,162.98CNY

  • Detail

70419-06-6SDS

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 (2S)-nonan-2-ol

1.2 Other means of identification

Product number -
Other names (S)-Nonan-2-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:70419-06-6 SDS

70419-06-6Relevant articles and documents

Catalytic Asymmetric Addition of Organolithium Reagents to Aldehydes

Veguillas, Marcos,Solà, Ricard,Shaw, Luke,Maciá, Beatriz

, p. 1788 - 1794 (2016/04/05)

Herein we report an efficient catalytic system for the titanium-promoted enantioselective addition of organolithium reagents to aldehydes, based on chiral Ar-BINMOL ligands. Unprecedented yields and enantioselectivities are achieved in the alkylation reactions of aliphatic aldehydes. Remarkably, methyllithium can be added to a wide variety of aromatic and aliphatic aldehydes, providing versatile chiral methyl carbinol units in a simple one-pot procedure under mild conditions and in very short reaction times.

Catalytic enantioselective addition of methyltriisopropoxititanium to aldehydes

Veguillas, Marcos,Solà, Ricard,Fernández-Iba?ez, M. ángeles,Maciá, Beatriz

, p. 643 - 648 (2016/07/11)

An efficient catalyst for the enantioselective synthesis of chiral methyl carbinols from aldehydes is presented. The system uses methyltriisopropoxytitanium as a nucleophile and a readily available binaphthyl derivative as a chiral ligand. The enantioselective methylation of both aromatic and aliphatic aldehydes proceeds with good yields and high enantioselectivities under mild conditions.

Identification of key residues in Debaryomyces hansenii carbonyl reductase for highly productive preparation of (S)-aryl halohydrins

Xu, Guo-Chao,Shang, Yue-Peng,Yu, Hui-Lei,Xu, Jian-He

supporting information, p. 15728 - 15731 (2015/11/02)

Key residues of Debaryomyces hansenii carbonyl reductase in the determination of the reducing activity towards aryl haloketones were identified through combinatorial mutation of conserved residues. This study provides a green and efficient biocatalyst for the synthesis of (S)-aryl halohydrins.

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