Welcome to LookChem.com Sign In|Join Free

CAS

  • or

28860-75-5

Post Buying Request

28860-75-5 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

28860-75-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28860-75-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,8,6 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 28860-75:
(7*2)+(6*8)+(5*8)+(4*6)+(3*0)+(2*7)+(1*5)=145
145 % 10 = 5
So 28860-75-5 is a valid CAS Registry Number.

28860-75-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (6E)-bicyclo[6.1.0]non-6-ene-9-carboxylate

1.2 Other means of identification

Product number -
Other names Bicyclo<6.1.0>non-2-en-9-carbonsaeure-ethylester

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:28860-75-5 SDS

28860-75-5Relevant articles and documents

Catalytic cyclopropanation with transition metal salts of soluble polyethylene carboxylates

Bergbreiter, David E.,Morvant, Mark,Chen, Bushi

, p. 2731 - 2734 (1991)

Syntheses of Rh(II) carboxylate salts of terminally funcfionalized polyethylene carboxylic acids arc described. These polymer-bound transition metals are homogeneous catalysts for cyclopropanation of alkenes at 100°C and have activities and selectivities like transition metal acetates but are quantitatively recoverable at 25°C.

Thermal valence isomerization of cis-fused bicyclic cyclobutenes. A study of orbital symmetry control

Dauben, William G.,Michno, Drake M.

, p. 2284 - 2292 (2007/10/19)

This study shows that thermally promoted valence isomerizations of cis-fused bicyclic cyclobutenes, when free of steric constraint, yield products arising from both orbital symmetry allowed conrotatory openings of the labile σ bond in the cyclobutene ring. In the case of the related vinylcyclobutenes, one conrotatory mode produces a stable cis,trans,cis monocyclic triene whereas fission in the other allowed sense affords a thermally labile trans,cis,cis monocyclic triene which, in turn, cyclizes to yield a cyclohexadiene derivative. The product distributions are evaluated in terms of secondary orbital interactions.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 28860-75-5