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199387-77-4

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199387-77-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 199387-77-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,3,8 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 199387-77:
(8*1)+(7*9)+(6*9)+(5*3)+(4*8)+(3*7)+(2*7)+(1*7)=214
214 % 10 = 4
So 199387-77-4 is a valid CAS Registry Number.

199387-77-4SDS

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 6-(aminomethyl)naphthalen-2-ol

1.2 Other means of identification

Product number -
Other names 6-aminomethyl-naphthalen-2-ol

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:199387-77-4 SDS

199387-77-4Relevant articles and documents

Sulfonamide derivatives for the treatment of diseases

-

Page/Page column 31, (2008/06/13)

The invention relates to compounds of formula (1) and to processes for the preparation of, intermediates used in the preparation of, compositions containing and the uses of, such derivatives. The compounds according to the present invention are useful in

A proton-transfer probe of a polymer-water interface. 2-Naphthol-labeled poly(isopropyl)acrylamide

Linares-Samaniego, Sandra,Tolbert, Laren M.

, p. 9974 - 9979 (2007/10/03)

Phase transitions in poly(N-isopropylacrylamide) (PNIPAM) covalently labeled with a 2-naphthol were examined by steady-state and time-resolved spectroscopy. 2-Naphthol undergoes excited-state proton transfer (ESPT) at a rate that is dependent upon water concentration in aqueous solvent systems. Upon conversion to the phase-separated state in naphthol-labeled PNIPAM, the efficiency of excited-state proton transfer diminished, consistent with formation of a globular phase in which exposure of the probe molecules to the water phase was reduced.

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