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13591-58-7

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13591-58-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13591-58-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,9 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13591-58:
(7*1)+(6*3)+(5*5)+(4*9)+(3*1)+(2*5)+(1*8)=107
107 % 10 = 7
So 13591-58-7 is a valid CAS Registry Number.

13591-58-7 Well-known Company Product Price

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  • Sigma-Aldrich

  • (73443)  Tin(II)ionophoreII  Selectophore, function tested

  • 13591-58-7

  • 73443-50MG

  • 3,790.80CNY

  • Detail

13591-58-7SDS

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 6-(4-nitrophenyl)-2,4-diphenyl-3,5-diazabicyclo[3.1.0]hex-2-ene

1.2 Other means of identification

Product number -
Other names 2,4-Diphenyl-6-p-nitrophenyl-1,3-diazabicyclo<3.1.0>hex-3-en

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:13591-58-7 SDS

13591-58-7Downstream Products

13591-58-7Relevant academic research and scientific papers

Two 1,3-Diazabicyclo[3.1.0]hex-3-enes with a 'Tripod' core

Mahmoodi, Nosrat O.,Tabatabaeian, Khalil,Kiyani, Hamzeh

experimental part, p. 536 - 542 (2012/05/04)

The photochromic 1,3-diazabiclyclo[3.1.0]hex-3-enes 5 and 6 were synthesized from two premade tris-aldehydes and two premade aziridinyl ketones and characterized (Scheme 1). Their spectra showed structurei-photochromic behavior relationships (SPBR), which were analyzed. Copyright

AZIRIDINYL KETONES AND THEIR CYCLIC ANILS. 10. 2,4,6-TRIARYL-1,3-DIAZABICYCLOHEX-3-ENES

Orlov, V. D.,Kaluski, Z.,Figas, E.,Vorob'eva, N. P.,Bakumenko, A. I.,Yaremenko, F. G.

, p. 849 - 854 (2007/10/02)

2,4,6-Triaryl-1,3-diazabicyclohex-3-enes were prepared by the reaction of α,β-dibromochalcones with aromatic aldehydes and ammonia.The exo- and endo-isomers were isolated and characterized.X-ray structural analysis of the endo-6-(4-nitrophenyl)-2,4

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