Cas 1005420-89-2,3-(4-aminophenyl)prop-2-ynenitrile

1005420-89-2

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Basic information

Product Name: 3-(4-aminophenyl)prop-2-ynenitrile
Synonyms: 3-(4-aminophenyl)prop-2-ynenitrile
CAS NO:1005420-89-2
Molecular Formula:
Molecular Weight: 142.16
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 3-(4-aminophenyl)prop-2-ynenitrile(CAS DataBase Reference)
NIST Chemistry Reference: 3-(4-aminophenyl)prop-2-ynenitrile(1005420-89-2)
EPA Substance Registry System: 3-(4-aminophenyl)prop-2-ynenitrile(1005420-89-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1005420-89-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1005420-89-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,5,4,2 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1005420-89:
(9*1)+(8*0)+(7*0)+(6*5)+(5*4)+(4*2)+(3*0)+(2*8)+(1*9)=92
92 % 10 = 2
So 1005420-89-2 is a valid CAS Registry Number.

1005420-89-2Upstream product

1005420-89-2Downstream Products

1005420-89-2Relevant academic research and scientific papers

New strong organic acceptors by cycloaddition of TCNE and TCNQ to donor-substituted cyanoalkynes

Reutenauer, Philippe,Kivala, Milan,Jarowski, Peter D.,Boudon, Corinne,Gisselbrecht, Jean-Paul,Gross, Maurice,Diederich, Francois

, p. 4898 - 4900 (2007)

Donor-substituted 1,1,2,4,4-pentacyanobuta-1,3-dienes and a cyclohexa-2,5-diene-1,4-diylidene-expanded derivative were prepared by a [2 + 2] cycloaddition of tetracyanoethene (TCNE) or 7,7,8,8-tetracyanoquinodimethane (TCNQ) to anilino-substituted cyanoal

MAPN: First-in-class reagent for kinetically resolved thiol-to-thiol conjugation

Koniev, Oleksandr,Kolodych, Sergii,Baatarkhuu, Zoljargal,Stojko, Johann,Eberova, Jitka,Bonnefoy, Jean-Yves,Cianférani, Sarah,Van Dorsselaer, Alain,Wagner, Alain

, p. 1863 - 1867 (2015)

Thiols are among the most frequently used functional groups in the field of bioconjugation. While there exists a variety of heterobifunctional reagents that allow for coupling thiols to other functions (e.g., amines, carboxylic acids), there is no specifi

3-ARYL PROPIOLONITRILE COMPOUNDS FOR THIOL LABELING

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Paragraph 0172-0173; 0206, (2016/06/13)

The present invention relates to a process for labeling compounds comprising thiol moieties with 3-arylpropiolonitrile compounds, to 3-arylpropiolonitrile compounds substituted with tag moieties and to specific 3-arylpropiolonitrile linkers.

3-aryl propiolonitrile compounds for thiol labeling

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Page/Page column, (2015/01/18)

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