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102423-16-5

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102423-16-5 Usage

Chemical class

Belongs to the benzotriazole class of organic compounds.

Molecular weight

245.23 g/mol

Appearance

It is typically a solid or liquid, depending on the specific formulation and conditions.

Photoinitiator

Commonly used as a photoinitiator in the polymer industry to initiate and control the polymerization process.

UV absorber

Utilized as a UV absorber in various applications, such as coatings, adhesives, and plastics, to provide protection from the harmful effects of ultraviolet radiation.

Applications

Has potential applications in the fields of organic synthesis and medicinal chemistry.

Stability

Generally stable under normal conditions, but may decompose upon exposure to heat, light, or other harsh conditions.

Solubility

Soluble in common organic solvents, such as ethanol, methanol, and acetone.

Reactivity

May react with strong acids, strong bases, or other reactive chemicals, leading to unwanted side reactions or degradation of the compound.

Safety

It is important to handle this compound with care, as it may have potential health hazards or environmental concerns. Appropriate safety measures should be taken during its use and disposal.

Check Digit Verification of cas no

The CAS Registry Mumber 102423-16-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,4,2 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 102423-16:
(8*1)+(7*0)+(6*2)+(5*4)+(4*2)+(3*3)+(2*1)+(1*6)=65
65 % 10 = 5
So 102423-16-5 is a valid CAS Registry Number.

102423-16-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name benzotriazol-1-yl prop-2-enyl carbonate

1.2 Other means of identification

Product number -
Other names allyl-1-benzotriazolyl carbonate

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:102423-16-5 SDS

102423-16-5Relevant articles and documents

Quinones as disease therapies

-

, (2008/06/13)

Novel quinones are provided, as well as compositions comprising these novel quinones. Methods of using the novel quinones in treatment of various indications including cancer are also provided.

Allyloxycarbonyl Group: A Versatile Blocking Group for Nucleotide Synthesis

Hayakawa, Yoshihiro,Kato, Hisatoyo,Uchiyama, Mamaoru,Kajino, Hisaki,Noyori, Ryoji

, p. 2400 - 2402 (2007/10/02)

Allyloxycarbonyl (AOC) is excellent for the protection of sugar hydroxyls and amino and imide moieties of nucleoside bases.The deblocking is easily performed by brief treatment with a palladium catalyst and a variety of nucleophiles at room temperature.

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