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137836-80-7

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137836-80-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137836-80-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,8,3 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 137836-80:
(8*1)+(7*3)+(6*7)+(5*8)+(4*3)+(3*6)+(2*8)+(1*0)=157
157 % 10 = 7
So 137836-80-7 is a valid CAS Registry Number.

137836-80-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyl-6-[(3-phenyl-2,4-dihydro-1,3-benzoxazin-6-yl)methyl]-2,4-dihydro-1,3-benzoxazine

1.2 Other means of identification

Product number -
Other names 2H-1,3-Benzoxazine,6,6'-methylenebis[3,4-dihydro-3-phenyl

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:137836-80-7 SDS

137836-80-7Downstream Products

137836-80-7Relevant articles and documents

Influence of electronic effects from bridging groups on synthetic reaction and thermally activated polymerization of bisphenol-based benzoxazines

Wang, Xiaoying,Chen, Feng,Gu, Yi

experimental part, p. 1443 - 1452 (2012/02/05)

Six bis-benzoxazines based on bisphenols with different bridging groups, -C(CH3)2-, -CH2-, -O-, -CO-, -SO2-, and single bond, were synthesized in toluene. The influence of electronic effects from bridging groups on ring-forming reaction and thermal ring-opening polymerization were relatively discussed in detail. Their structures were characterized by high-performance liquid chromatography, Fourier transform infrared, 1H NMR, differential scanning calorimetry, and elementary analysis. The quantum chemistry parameters of the bisphenols and bis-benzoxazines were calculated by molecular simulation. The results indicated that the electron-withdrawing groups inhibited the synthetic reaction by decreasing the charge density of α-Cs of bisphenols and increasing energy barriers of the synthetic reactions. However, the electron-withdrawing groups promoted the thermally activated polymerization, which resulted from their activation energy and curing temperature decrease by increasing the bond length and lowering the bond energy of C-O on oxazine rings. Besides, because of stronger electron-withdrawing sulfone group, there were more arylamine methylene Mannich bridge structure in the polybenzoxazine.

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