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14795-13-2

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14795-13-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14795-13-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,9 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 14795-13:
(7*1)+(6*4)+(5*7)+(4*9)+(3*5)+(2*1)+(1*3)=122
122 % 10 = 2
So 14795-13-2 is a valid CAS Registry Number.

14795-13-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N'-bis(2-chlorophenyl)methanediamine

1.2 Other means of identification

Product number -
Other names methylene-bis-ortho chloroaniline

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:14795-13-2 SDS

14795-13-2Relevant articles and documents

Interpretation of the mechanism of 3,3′-dichloro-4,4′-diamino diphenylmethane synthesis over HY zeolites

Ruan, Xiao,Wang, Qiang,Wei, Feng,Yang, Li,Zhao, Yingxian

, p. 34719 - 34728 (2020/10/12)

Catalytic activities of zeolites HY, Hβ and HZSM-5 in the heterogeneous synthesis of 3,3′-dichloro-4,4′-diaminodiphenyl methane (MOCA) fromo-chloroaniline and formaldehyde were pre-screened in an autoclave, and HY demonstrated better performance than others. Kinetic behaviors of MOCA synthesis over HY(11) were further investigated in a fixed bed continuous flow reactor, and under the conditions of the catalyst bed volume = 20 mL (8.14 g),n(o-chloroaniline) : n(HCHO) = 4 : 1, LHSV = 3.5 h?1, 0.5 MPa and 443 K, HCHO conversion and MOCA selectivity steadily fluctuated at high levels of 90-92% and 75-77% during 16 h, respectively. Catalysts were characterized by BET, NH3-TPD and XRD, products analyzed by HPLC, and reaction intermediates identified by LC/MS and1H NMR. The mechanism of MOCA synthesis has been interpreted in detail, which also suggested that deposition of basic intermediates on active sites and accumulation of polymeric by-products in pore channels of the catalyst could cause significant decay of HY(11) activity and selectivity under severe conditions. Supplementary tests on catalyst regeneration confirmed that the acidity and surface area of spent HY(11) could be well recovered after burning off the deposited by-products.

Method for preparing polyurethanes using 3,9-bis(2-hydrazidoethyl)-2-4,8,10-tetraoxaspiro-[5,5]-undecane as chain extender

-

, (2008/06/13)

Polyurethane is prepared by reacting a prepolymer having terminal isocyanate groups with 3,9-bis(2-hydrazidoethyl)-2,4,8,10-tetraoxaspiro-[5,5]-undecane.

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