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N-Methoxy-N-MethylcycloheptanecarboxaMide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

253429-08-2

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253429-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 253429-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,3,4,2 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 253429-08:
(8*2)+(7*5)+(6*3)+(5*4)+(4*2)+(3*9)+(2*0)+(1*8)=132
132 % 10 = 2
So 253429-08-2 is a valid CAS Registry Number.

253429-08-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methoxy-N-methyl-cycloheptanecarboxamide

1.2 Other means of identification

Product number -
Other names N-Methoxy-N-methylcycloheptanecarboxamide

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:253429-08-2 SDS

253429-08-2Downstream Products

253429-08-2Relevant academic research and scientific papers

Zn-ProPhenol Catalyzed Enantioselective Mannich Reaction of 2 H-Azirines with Alkynyl Ketones

Trost, Barry M.,Zhu, Chuanle

supporting information, p. 9683 - 9687 (2020/12/21)

The enantioselective Mannich reaction of 2H-azirines with alkynyl ketones is achieved under Zn-ProPhenol catalysis, delivering various aziridines with vicinal tetrasubstituted stereocenters in high yields with excellent enantioselectivities. The bimetalli

TRICYCLIC COMPOUND SERVING AS IMMUNOMODULATOR

-

Paragraph 0613-0614, (2019/01/04)

Provided are compounds of formula I and formula II or pharmaceutically acceptable salts of the compounds and pharmaceutical compositions thereof. The compounds of formula I and formula II or the pharmaceutically acceptable salts of the compounds provide indole 2,3-dioxygenase (IDO) inhibitory activity and are capable of treating IDO-mediated immunosuppressive diseases, such as infectious diseases or cancer.

Copper(I)-Catalyzed Enantioselective Nucleophilic Borylation of Aliphatic Ketones: Synthesis of Enantioenriched Chiral Tertiary α-Hydroxyboronates

Kubota, Koji,Osaki, Shun,Jin, Mingoo,Ito, Hajime

supporting information, p. 6646 - 6650 (2017/05/29)

A new method was developed for the first catalytic enantioselective borylation of aliphatic ketones. A variety of substrates reacted efficiently with bis(pinacolato)diboron in the presence of a copper(I)/chiral N-heterocyclic carbene complex catalyst to furnish optically active tertiary α-hydroxyboronates with moderate to high enantioselectivities (up to 94 % ee). Notably, the product could be converted into the chiral tertiary alcohol derivative using a stereospecific boron functionalization process. The theoretical study of the mechanism for the enantioselectivity is also described.

Piperidine derivatives as reuptake inhibitors

-

Page column 34-35, (2010/02/09)

The present invention provides compounds of formula (I) and a method of inhibiting the reuptake of serotonin and antagonizing the serotonin receptor which comprises administering to a subject in need of such treatment an effective amount of a compound of formula (I).

Piperidine derivatives as serotonine reuptake inhibitors

-

Page column 28, (2010/02/05)

The present invention provides compounds of formula I and a method of inhibiting the reuptake of serotonin, antagonizing the 5-HT1Areceptor and antagonizing the 5-HT2Areceptor which comprises administering to a subject in need of such treatment an effective amount of a compound of formula I.

Piperidine derivatives having effects on serotonin related systems

-

, (2008/06/13)

The present invention provides the compounds of the following formula: Wherein the variables are as defined in the specification and a method for inhibiting the reuptake of seretonin, antagonizing the 5-HT1Areceptor and antagonizing the 5-HT2Areceptor which comprises administering to a subject in need of such treatment an effective amount of the compound of above formula.

Azepine derivatives having effects on serotonin related systems

-

, (2008/06/13)

The present invention provides compounds of formula I and a method of inhibiting the reuptake of serotonin, antagonizing the 5-HT1Areceptor and antagonizing the 5-HT2Areceptor which comprises administering to a subject in need of suc

Pyrrolidine and pyrroline derivatives having effects on serotonin related systems

-

Page column 31, (2010/02/05)

The present invention provides the compounds of the following formula (I): and a method for inhibiting the reuptake of seretonin, antagonizing the 5-HT1Areceptor and antagonizing the 5-HT2Areceptor which comprises administering to a subject in need of such treatment an effective amount of formula (I).

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