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553-17-3

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553-17-3 Usage

Uses

Guaiacol Carbonate is used in method for preparing Polycarbonate Polyol and compound comprising the Polycarbonate Polyol.

Purification Methods

Crystallise the carbonate from EtOH. It is estimated by bromination to the monobromo guaiacol carbonate m 178o (from EtOH) [Chernoff J Am Chem Soc 51 3073 1929]. [Beilstein 6 H 776, 6 I 386, 6 II 784, 6 III 4233.]

Check Digit Verification of cas no

The CAS Registry Mumber 553-17-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,5 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 553-17:
(5*5)+(4*5)+(3*3)+(2*1)+(1*7)=63
63 % 10 = 3
So 553-17-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H14O5/c1-17-11-7-3-5-9-13(11)19-15(16)20-14-10-6-4-8-12(14)18-2/h3-10H,1-2H3

553-17-3 Well-known Company Product Price

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  • Alfa Aesar

  • (L12825)  Bis(2-methoxyphenyl) carbonate, 98%   

  • 553-17-3

  • 5g

  • 508.0CNY

  • Detail
  • Alfa Aesar

  • (L12825)  Bis(2-methoxyphenyl) carbonate, 98%   

  • 553-17-3

  • 25g

  • 2037.0CNY

  • Detail

553-17-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Guaiacol carbonate

1.2 Other means of identification

Product number -
Other names bis(2-methoxyphenyl) 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:553-17-3 SDS

553-17-3Relevant articles and documents

The reactions of difluorodiiodomethane with nucleophiles

Guo, Yong,Chen, Qing-Yun

, p. 105 - 109 (2007/10/03)

Treatment of difluorodiiodomethane with phenoxides (ArO-) in DMF at room temperature gives ArOCF2I in 7-15%, the carbonates (ArOCO2Ar) being the major products, while with thiophenoxides affords difluoromethylene derivativ

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