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13004-86-9

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13004-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13004-86-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,0 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13004-86:
(7*1)+(6*3)+(5*0)+(4*0)+(3*4)+(2*8)+(1*6)=59
59 % 10 = 9
So 13004-86-9 is a valid CAS Registry Number.

13004-86-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,5-diphenyl-1,5-bis(phenylsulfanyl)pentan-3-one

1.2 Other means of identification

Product number -
Other names 1,5-Diphenyl-1,5-bis-phenylmercapto-pentan-3-on

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:13004-86-9 SDS

13004-86-9Downstream Products

13004-86-9Relevant articles and documents

Synthesis and antibacterial and antifungal evaluation of some chalcone based sulfones and bisulfones

Konduru, Naveen Kumar,Dey, Sunita,Sajid, Mohammad,Owais, Mohammad,Ahmed, Naseem

, p. 23 - 30 (2013/03/13)

Two series of chalcone based sulfone and bisulfone derivatives were synthesized using chalcone, thiophenol and sodium metal at room temperature, followed by oxidation of chalcone sulfides with m-CPBA at 0 °C in a novel method. Both sulfones and bisulfones

Conjugate addition of indoles and thiols with electron-deficient olefins catalyzed by Bi(OTf)3

Alam, M. Mujahid,Varala, Ravi,Adapa, Srinivas R.

, p. 5115 - 5119 (2007/10/03)

Conjugate addition of indoles and thiols with a variety of electron-deficient olefins mediated by a catalytic amount of Bi(OTf)3 at ambient temperature to afford the corresponding Michael adducts in good to excellent yields with high selectivity is reported.

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