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Cyclohexanamine, N-3-butenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61907-83-3

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61907-83-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61907-83-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,0 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61907-83:
(7*6)+(6*1)+(5*9)+(4*0)+(3*7)+(2*8)+(1*3)=133
133 % 10 = 3
So 61907-83-3 is a valid CAS Registry Number.

61907-83-3SDS

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 N-but-3-enylcyclohexanamine

1.2 Other means of identification

Product number -
Other names Cyclohexanamine,N-3-butenyl

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:61907-83-3 SDS

61907-83-3Downstream Products

61907-83-3Relevant academic research and scientific papers

N-heterocycles from chromium aminocarbenes

Déry, Martin,Assouvie, Kevin,Heinrich, Nora,Rajotte, Isabelle,Lefebvre, Louis-Philippe D.,Legault, Marc-André,Spino, Claude

supporting information, p. 1312 - 1315 (2015/03/14)

The initial [2 + 2]-cycloadduct between a chromium aminocarbene and a tethered alkene undergoes a β-hydrogen elimination very efficiently when triphenylphosphine is added as a ligand. The reaction gives cyclic enamines or homoenamines depending on the sub

Monoalkylation of Primary Aliphatic Amines via N-Alkyl-N-(alkylthiomethyl)ammonium Chlorides. Evidence for the Formation of Stable N-Methylenealkylamines

Barluenga, Jose,Bayon, Ana M.,Asensio, Gregorio

, p. 427 - 428 (2007/10/02)

Monomeric N-methylenealkylamines (3), formed from N-alkyl-N-(alkylthiomethyl)ammonium chlorides (5) are stable at -60 deg C and may be trapped with organometallic reagents to provide the N,N-dialkylamines (8).

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