Skip to Content
Merck
All Photos(2)

Documents

Safety Information

916722

Sigma-Aldrich

Phenyl-(benzo)phenothiazine

Synonym(s):

Ph-benzoPTZ, Phenyl-benzo[b]phenothiazine

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Empirical Formula (Hill Notation):
C22H15NS
CAS Number:
1320277-85-7
Molecular Weight:
325.43
UNSPSC Code:
12352200
NACRES:
NA.22

form

powder

Quality Level

100

reaction suitability

reaction type: Photocatalysis
reagent type: catalyst

mp

160-167 °C

Related Categories

Application

Phenyl-(benzo)phenothiazine is an organic photo-catalyst used in synthesis of small molecules as well as polymerization reactions.

Product can be used with our line of photoreactors: Including Penn PhD (Z744035) & SynLED 2.0 (Z744080)

Other Notes

Design, Synthesis, and Application of Highly Reducing Organic Visible-Light Photocatalysts

Organophotoredox-Catalyzed Decarboxylative C(sp3)-O Bond Formation

related product

Product No.
Description
Pricing

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

916722-BULK:
916722-VAR:
916722-250MG:
916722-100MG:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Shotaro Shibutani et al.
Journal of the American Chemical Society, 142(3), 1211-1216 (2020-01-04)
This manuscript reports a visible-light-mediated organosulfide catalysis that enables the decarboxylative coupling between simple aliphatic alcohol and tertiary or secondary alkyl carboxylic acid-derived redox active esters to produce a C(sp3)-O-C(sp3) fragment. Results of the coupling using other heteroatom nucleophiles such
Dan Liu et al.
Organic letters, 20(18), 5700-5704 (2018-09-07)
A series of inexpensive, easily tunable, and highly reducing organic photocatalysts (PCs) that exhibit strong absorption in the visible region are described. Time-dependent density functional theory calculations were applied to corroborate the experimental observations and explain the relationship between the

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service