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86660-74-4

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86660-74-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86660-74-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,6,6 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86660-74:
(7*8)+(6*6)+(5*6)+(4*6)+(3*0)+(2*7)+(1*4)=164
164 % 10 = 4
So 86660-74-4 is a valid CAS Registry Number.

86660-74-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-azido-4-(cyclohexen-1-yl)thiophene

1.2 Other means of identification

Product number -
Other names 3-(cyclohex-1-enyl)-4-azidothiophen

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:86660-74-4 SDS

86660-74-4Downstream Products

86660-74-4Relevant articles and documents

Thermal Decomposition of o-Azidobithienyls

Zanirato, Paolo,Spagnolo, Piero,Zanardi, Giuseppe

, p. 2551 - 2554 (2007/10/02)

Thermal decomposition of the six possible o-azidobithienyls (1)-(6) has been investigated as a possible source of the hitherto unknown dithienopyrrole ring system.It was found that the nature and yield of products and the temperature required for decomposition are strongly dependent on the structure of the starting azides. 3-Azido-2,2'-bithienyl (1) and 3-azido-2,3'-bithienyl (2) gave 4H-dithienopyrrole (7) and 4H-dithienopyrrole (8), respectively, in very good yields. 4-Azido-3,3'-dithienyl (3) and 4-azido-2',3-bithienyl (4) were relatively stable under the same conditions, but polymer ic materials were obtained when the thermal decomposition was performed under more vigorous conditions.By contrast, 2-azido-3,3'-bithienyl (5) and 2-azido-2',3-bithienyl (6) extrude nitrogen at room temperature resulting in ring-opening fragmentation.Thermolysis of 3-azido-2-cyclohex-1-enylthiophen (11) and 4-azido-3-cyclohex-1-enylthiophen (12) were also investigated to elucidate the different behavioural patterns exhibited by the 3-azidothienyl derivatives.

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