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(E)-1,5-Heptadiene is an organic compound with the molecular formula C7H12. It is a colorless liquid with a strong, pungent odor. This alkene features a double bond between the first and fifth carbon atoms in a linear arrangement, giving it the E (entgegen) configuration, which means the two largest groups are on opposite sides of the double bond. It is an important intermediate in the synthesis of various chemicals and can be used in the production of perfumes, pharmaceuticals, and other organic compounds. (E)-1,5-Heptadiene is also known for its reactivity, as it readily undergoes addition reactions, making it a valuable building block in organic chemistry.

7736-22-3

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7736-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7736-22-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,3 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7736-22:
(6*7)+(5*7)+(4*3)+(3*6)+(2*2)+(1*2)=113
113 % 10 = 3
So 7736-22-3 is a valid CAS Registry Number.

7736-22-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-1,5-heptadiene

1.2 Other means of identification

Product number -
Other names hepta-1,5t-diene

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:7736-22-3 SDS

7736-22-3Relevant academic research and scientific papers

EVIDENCE FOR A SINGLE ELECTRON TRANSFER MECHANISM IN REACTIONS OF LITHIUM DIORGANOCUPRATES WITH ORGANIC HALIDES

Ashby, E. C.,DePriest, R. N.,Tuncay, A.,Srivastava, Sushil

, p. 5251 - 5254 (2007/10/02)

It has been demonstrated by means of spectroscopic studies involving cyclizable alkyl halides that lithium dimethylcuprate can react with organic halides by a single electron transfer pathway.

Catalyzed cross-coupling of allyl bromides with allyl tin reagents

Godschalx, James,Stille

, p. 2599 - 2602 (2007/10/02)

The reaction of allyl bromides with allyl tin reagents, catalyzed by palladium or zinc chloride gives cross-coupled products without allylic transpostion in the allyl halide partner but with predominate allylic rearrangement from the tin partner.

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