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Heptanal, 2-(phenylmethoxy)-, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84994-61-6

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84994-61-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84994-61-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,9,9 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 84994-61:
(7*8)+(6*4)+(5*9)+(4*9)+(3*4)+(2*6)+(1*1)=186
186 % 10 = 6
So 84994-61-6 is a valid CAS Registry Number.

84994-61-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-phenylmethoxyheptanal

1.2 Other means of identification

Product number -
Other names -

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:84994-61-6 SDS

84994-61-6Relevant academic research and scientific papers

An enantioselective approach to 2-alkyl substituted tetrahydroquinolines: Total synthesis of (+)-angustureine

Garg, Yuvraj,Gahalawat, Suraksha,Pandey, Satyendra Kumar

, p. 38846 - 38850 (2015/05/20)

A simple and highly efficient synthetic approach to enantiopure 2-alkyl substituted tetrahydroquinoline 1 skeleton from aldehydes as starting materials and its application to the total synthesis of (+)-angustureine 2 is described. Key transformations incl

Enantioselective syntheses of (+)- and (-)-phaseolinic acid

Jacobi, Peter A.,Herradura, Prudencio

, p. 8297 - 8300 (2007/10/03)

(+)- and (-)-Phaseolinic acid (1) have been prepared in an enantioselective fashion from acetylenic acid 26 (or ent-26) by a three step sequence involving lactonization, epimerization at C3, and oxidative cleavage. 26 was obtained as a single enantiomer using a Nicholas-Schreiber reaction.

Transformations of Tartaric Acid. Complementary Methods for the Synthesis of Optically Active α-Hydroxyaldehyde Derivatives

Achmatowicz, Barbara,Wicha, Jerzy

, p. 267 - 276 (2007/10/02)

Methods for the synthesis of (R)- and (S)-2-benzyloxy and 2-(t-butyldiphenylsilyloxy)-aldehydes from optically active tartaric acids are described.

TRANSFORMATION OF TARTARIC ACID: A FACILE SYNTHESIS OF DERIVATIVES OF OPTICALLY ACTIVE α-HYDRXYOALDEHYDES

Achmatowicz, Barbara,Wicha, Jerzy

, p. 2999 - 3002 (2007/10/02)

Methods for synthesis of (R)- and (S)-2-benzyloxy- and 2-(t-butyldiphenylsilyloxy)-aldehydes from optically active tartaric acids are described.

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