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16078-25-4

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16078-25-4 Usage

General Description

(R)-(-)-3-Methylpiperidine is a chemical compound that belongs to the class of piperidines, which are organic compounds containing a six-membered ring derived from piperidine. (R)-(-)-3-METHYLPIPERIDINE is a chiral molecule, meaning it has a non-superimposable mirror image, and the (R)-(-)-enantiomer is the specific optical isomer being referred to. It is used in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. This chemical is also known for its use in the production of bactericides and fungicides. Additionally, it is often employed as a building block for the synthesis of various biologically active molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 16078-25-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,7 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16078-25:
(7*1)+(6*6)+(5*0)+(4*7)+(3*8)+(2*2)+(1*5)=104
104 % 10 = 4
So 16078-25-4 is a valid CAS Registry Number.

16078-25-4SDS

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 (3R)-3-methylpiperidine

1.2 Other means of identification

Product number -
Other names Piperidine,3-methyl-,(3R)

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:16078-25-4 SDS

16078-25-4Relevant articles and documents

Efficient asymmetric hydrogenation of pyridines

Glorius, Frank,Spielkamp, Nick,Holle, Sigrid,Goddard, Richard,Lehmann, Christian W.

, p. 2850 - 2852 (2004)

Up to four stereocenters can be created efficiently in a single step by the asymmetric hydrogenation of oxazolidinone-substituted pyridines (see scheme). Furthermore, selective chirality transfer and nondestructive cleavage of the chiral auxiliary occur under the same reaction conditions, making an additional cleavage step unnecessary.

Synthesis of: N -heterocycles from diamines via H2-driven NADPH recycling in the presence of O2

Al-Shameri, Ammar,Borlinghaus, Niels,Weinmann, Leonie,Scheller, Philipp N.,Nestl, Bettina M.,Lauterbach, Lars

, p. 1396 - 1400 (2019/03/26)

Herein, we report an enzymatic cascade involving an oxidase, an imine reductase and a hydrogenase for the H2-driven synthesis of N-heterocycles. Variants of putrescine oxidase from Rhodococcus erythropolis with improved activity were identified. Substituted pyrrolidines and piperidines were obtained with up to 97% product formation in a one-pot reaction directly from the corresponding diamine substrates. The formation of up to 93% ee gave insights into the specificity and selectivity of the putrescine oxidase.

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