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46711-49-3

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46711-49-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 46711-49-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,7,1 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 46711-49:
(7*4)+(6*6)+(5*7)+(4*1)+(3*1)+(2*4)+(1*9)=123
123 % 10 = 3
So 46711-49-3 is a valid CAS Registry Number.

46711-49-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name naphthalene-2,6-dicarboxamide

1.2 Other means of identification

Product number -
Other names Naphthalin-2,6-dicarbamid

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:46711-49-3 SDS

46711-49-3Downstream Products

46711-49-3Relevant articles and documents

Design, synthesis, and characterization of a novel hexa-azacyclophane and interactions with d(CGCA3T3GCG)2, ctDNA and T4DNA

Bruice, Thomas C.,Yip, Yu Chi,Blasko, Andrei,Lightstone, Felice C.,Browne, Kenneth A.,Petyak, Mark E.,Luo, Jia

, p. 8105 - 8120 (1997)

A novel polyazacyclophane hexa-amine (1) has been designed, synthesized and characterized by X-ray crystallography, 1H NMR and fluorescence spectroscopy. 1 has the structural shape and disposition of charges complementary to the major groove of B-DNA. Acid dissociation constants for the protonated 1 were pK(a1)(D) = 4.8 and pK(a2)(D) = 8.5. Equilibrium constants for the binding of 1 to ctDNA and T4 DNA were 1.2 x 105 and 1.8 x 106, respectively.

Corresponding amine nitrile and method of manufacturing thereof

-

Paragraph 0122; 0123; 0125, (2018/05/24)

The invention relates to a preparation method of nitrile. Compared with the prior art, the preparation method has the characteristics of obvious reduction of the usage amount of ammonia sources, low environmental pressure, low energy consumption, low production cost, high purity and yields of nitrile products, and the like, and can be used for obtaining nitrile with a more complex structure. The invention also relates to a method for preparing corresponding amine with nitrile.

Cyclic imino derivatives and pharmaceutical compositions containing them

-

, (2008/06/13)

The invention relates to cyclic imino compounds which have, inter alia, valuable pharmacological properties, especially inhibitory effects on cell aggregation, pharmaceutical compositions which contain these compounds and processes for preparing them.

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