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62227-61-6

Benzamide, N-(1-ethynylbutyl)-, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 62227-61-6 Structure

  • Basic information

    1. Product Name: Benzamide, N-(1-ethynylbutyl)-, (R)-
    2. Synonyms:
    3. CAS NO:62227-61-6
    4. Molecular Formula: C13H15NO
    5. Molecular Weight: 201.268
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 62227-61-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzamide, N-(1-ethynylbutyl)-, (R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzamide, N-(1-ethynylbutyl)-, (R)-(62227-61-6)
    11. EPA Substance Registry System: Benzamide, N-(1-ethynylbutyl)-, (R)-(62227-61-6)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 62227-61-6(Hazardous Substances Data)

62227-61-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62227-61-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,2 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62227-61:
(7*6)+(6*2)+(5*2)+(4*2)+(3*7)+(2*6)+(1*1)=106
106 % 10 = 6
So 62227-61-6 is a valid CAS Registry Number.

62227-61-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-((R)-1-Ethynyl-butyl)-benzamide

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:62227-61-6 SDS

62227-61-6Upstream product

62227-61-6Downstream Products

62227-61-6Relevant articles and documents

Enantioselective radical alkynylation of C(sp3)-H bonds using sulfoximine as a traceless chiral auxiliary

Nagatomo, Masanori,Yoshioka, Shun,Inoue, Masayuki

, p. 120 - 123 (2015)

Enantioselective alkynylation of C(sp3)-H bonds adjacent to a nitrogen atom has been achieved using only chiral p-tolyl tert-butyldimethylsilylethynyl sulfoximine and benzophenone under photo-irradiation conditions. A twocarbon alkyne unit was chemo- and enantioselectively transferred at the nitrogen-substituted methylene to produce the optically active propargylic amines of various structures. Remarkably, the NH-unprotected sulfoximine group efficiently transmits its stereochemical information to the product and functions as a traceless chiral auxiliary.

A New Class of Redox Isomerization of N-Alkylpropargylamines into N-Alkylideneallylamines Catalyzed by a ReBr(CO)5/Amine N-oxide System

Fukumoto, Yoshiya,Okazaki, Natsuki,Chatani, Naoto

supporting information, p. 1760 - 1765 (2019/03/11)

Redox isomerization reaction wherein N-alkylpropargylamines are converted into N-alkylideneallylamines in the presence of rhenium(I) complexes as catalysts is described. Among the additives tested, certain pyridine N-oxides and tertiary amine N-oxides wer

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