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ethyl 2-(1-formylcyclohexyl)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

460711-33-5

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460711-33-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 460711-33-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,0,7,1 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 460711-33:
(8*4)+(7*6)+(6*0)+(5*7)+(4*1)+(3*1)+(2*3)+(1*3)=125
125 % 10 = 5
So 460711-33-5 is a valid CAS Registry Number.

460711-33-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (1-formylcyclohexyl)acetate

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:460711-33-5 SDS

460711-33-5Relevant academic research and scientific papers

SPIRO-LACTAM NMDA RECEPTOR MODULATORS AND USES THEREOF

-

Page/Page column 27-28, (2019/08/26)

Disclosed are compounds having potency in the modulation of NMDA receptor activity. Such compounds can be used in the treatment of conditions such as depression and related disorders as well as other disorders.

N-heterocyclic carbene-catalyzed Ireland-Coates claisen rearrangement: Synthesis of functionalized β-lactones

Candish, Lisa,Lupton, David W.

supporting information, p. 58 - 61 (2013/02/25)

The N-heterocyclic carbene (NHC)-catalyzed Claisen rearrangement of hybrid Ireland-Coates structures has been achieved, allowing the stereoselective synthesis of highly functionalized β-lactones. The reaction proceeds with high diastereoselectivity (>20:1

Process for the preparation of gabapentin

-

Page/Page column 3, (2008/06/13)

A simple, efficient, environmentally improved and economical process for preparing gabapentin, involving enamine alkylation as the key step is disclosed.

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