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Sulfamic acid, (4-methoxyphenyl)-, monosodium salt is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64808-25-9

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64808-25-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64808-25-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,8,0 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 64808-25:
(7*6)+(6*4)+(5*8)+(4*0)+(3*8)+(2*2)+(1*5)=139
139 % 10 = 9
So 64808-25-9 is a valid CAS Registry Number.

64808-25-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium 4-methoxyphenylsulfamate

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:64808-25-9 SDS

64808-25-9Relevant academic research and scientific papers

HETEROCYCLIC DIHYDROPYRIMIDINE COMPOUNDS

-

Page/Page column 65-66, (2008/06/13)

Novel heterocyclic dihydropyrimidine compounds useful as inhibitors of potassium channel function (especially inhibitors of the Kv1 subfamily of voltage gated K+ channels, especially inhibitors Kv1.5 which has been linked to the ultra rapidly activating d

The Photochemistry of para-Substituted Phenylsulphamates - Photo-Fries Rearrangements

Lally, John M.,Spillane, William J.

, p. 803 - 807 (2007/10/02)

The photolysis (254 nm) of a series of para-substituted phenylsulphamates, XC6H4NHSO3Na in degassed methanolic solutions has been examined.For 1a and 1b photo-Fries type rearrangements to sulphonic acids and photodegradation to anilines have been observed.The halogenosulphamates 1c-1e do not rearrange but degrade to anilines and are photosolvolysed to p-methoxyphenylsulphamic acid.No notable spectral changes took place during the irradiation of 1f over relatively long period.Substrate concentration studies, radical scavenging and sensitization and quenching experiments on 1b indicate that, as previously found for 1a, its photolysis involves an intramolecular radical mechanism with the participation of two triplet states.

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