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25116-80-7

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25116-80-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25116-80-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,1,1 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 25116-80:
(7*2)+(6*5)+(5*1)+(4*1)+(3*6)+(2*8)+(1*0)=87
87 % 10 = 7
So 25116-80-7 is a valid CAS Registry Number.

25116-80-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-piperidin-1-ylsulfanylpiperidine

1.2 Other means of identification

Product number -
Other names Piperidine,1,1'-thiodi

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:25116-80-7 SDS

25116-80-7Relevant articles and documents

A new method for the synthesis of N,N′-thiobisamines

Dudin

, p. 1796 - 1797 (2007/10/03)

Reaction of secondary amines (morpholine and piperidine) with sulfur and iodine afforded N,N′-thiobisamines in good yields.

Use of Piperidine-1-sulphenyl Chloride as a Sulphur-transfer Reagent in Reactions with Diamines: The Preparation of Sulphur-Nitrogen Heterocycles

Bryce, Martin R.

, p. 2591 - 2593 (2007/10/02)

The use of piperidine-1-sulphenyl chloride (3) as a sulphur-transfer reagent in reactions with diamines is described.The reactions of (3) with o-phenylenediamine yielded the dihydro-2,1,3-benzothiadiazole (6) and benzothiadiazole (7).Oxidation of (6) with m-chloroperoxybenzoic acid yielded (7).The reactions of (3) with 1,8-diaminonaphthalene and 1,4,5,8-tetra-aminonaphthalene yielded the 1,2,6-thiadiazine derivatives (14) and (16); possible mechanisms are discussed. 1,2-Diamino-N,N'-dimethylethane and (3) yielded the tetrahydrothiadiazole (17), whereas 1,3-diaminopropane and (3) afforded the novel N-S-N chain compound (19).The reactions of morpholine-1-sulphenyl chloride (4) with aromatic diamines gave the same products in low yields.

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