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1207-71-2

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1207-71-2 Usage

Uses

10H-Phenothiazine 5-Oxide is a by-product in the synthesis of Phenothiazine S,S-Dioxide (P297600). Phenothiazine S,S-Dioxide is a derivative of Phenothiazine (P318040), a key component of antipsychotic and antihistaminic drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 1207-71-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,0 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1207-71:
(6*1)+(5*2)+(4*0)+(3*7)+(2*7)+(1*1)=52
52 % 10 = 2
So 1207-71-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H9NOS/c14-15-11-7-3-1-5-9(11)13-10-6-2-4-8-12(10)15/h1-8,13H

1207-71-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 10H-phenothiazine 5-oxide

1.2 Other means of identification

Product number -
Other names phenothiazine sulfoxyde

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:1207-71-2 SDS

1207-71-2Related news

Luminescence properties of PPV-based conjugated polymers containing phenothiazine and PHENOTHIAZINE-5-OXIDE (cas 1207-71-2) units07/18/2019

The photo-physical and electroluminescent properties of five PPV-type conjugated polymers containing phenothiazine and phenothiazine-5-oxide moieties were studied by UV–vis, PL and EL methods. The polymers showed PL maxima in the range 546-553 nm in solution and is 574–589 nm in solid. Red shi...detailed

1207-71-2Relevant articles and documents

Ozonization of phenothiazine and its analogues

Matsui,Miyamoto,Shibata,Takase

, p. 2526 - 2530 (1984)

When phenothiazine and phenoxazine were ozonized in dichloromethane, the cation radicals and the ozonate anion radicals were detected, whereas, in the ozonization of phenoxathiin and thianthrene, these radicals were not observed. Formation of these radicals was more favorable as greater was the polarity of the solvent and lower was the oxidation potential of the substrate. Ozonization of phenothiazine and phenoxazine in polar solvents was explained by the electron-transfer mechanism accompanied by the electrophilic ozone attack, and that of phenoxathiin and thianthrene by the electrophilic ozone attack alone.

STRUCTURE AND HYDROLYTIC ACTIVITY OF N-VINYL DERIVATIVES OF PHENOTHIAZINE, CARBAZOLE AND ACRIDONE

Kurov, G. N.,Afonin, A. V.,Svyatkina, L. I.,Dmitrieva, L. L.,Pal'chuk, E. G.

, p. 403 - 405 (2007/10/02)

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