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92326-42-6

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92326-42-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92326-42-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,3,2 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 92326-42:
(7*9)+(6*2)+(5*3)+(4*2)+(3*6)+(2*4)+(1*2)=126
126 % 10 = 6
So 92326-42-6 is a valid CAS Registry Number.

92326-42-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(heptan-4-ylideneamino)heptan-4-imine

1.2 Other means of identification

Product number -
Other names diheptan-4-ylidenehydrazine

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:92326-42-6 SDS

92326-42-6Downstream Products

92326-42-6Relevant articles and documents

Photolysis of dipropyldiazirine and trapping of dipropylcarbene with piperidine

Tae, Eunju Lee,Platz, Matthew S.

, p. 2875 - 2878 (2007/10/03)

Photolysis (350 nm) of dipropyldiazirine in methylene chloride at 4°C produces a mixture of E and Z 3-heptene in 81% yield in an E/Z ratio of 1.8. Tetrapropylazine was formed in less than 5% yield. Photolysis of dipropyldiazirine in the presence of piperidine leads to the formation of a carbene-amine adduct. In the presence of 0.06 M piperidine the yield of adduct is 48%, the yield of E and Z 3-heptene is 47% and the E/Z ratio of 3- heptenes is 1.1. The results show that heptene is formed by three pathways. One pathway involves dipropylcarbene formed directly from the diazirine, the other pathways are attributed to ionic and photochemical reactions of 4- diazoheptane and to the excited state of the diazirine precursor. Dipropylcarbene can be easily intercepted with a simple trap. The yield of this process is limited by the efficiency with which the precursor forms the carbene.

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