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17994-26-2

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17994-26-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17994-26-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,9 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17994-26:
(7*1)+(6*7)+(5*9)+(4*9)+(3*4)+(2*2)+(1*6)=152
152 % 10 = 2
So 17994-26-2 is a valid CAS Registry Number.

17994-26-2SDS

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 bicyclo[2.2.1]hept-5-ene-2,3-dione

1.2 Other means of identification

Product number -
Other names 5-norbornene-2,3-dione

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:17994-26-2 SDS

17994-26-2Relevant articles and documents

A building BLOCK approach to bis-porphyrin cavity systems with convergent and divergent wall orientations

Johnston, Martin R,Gunter, Maxwell J,Warrener, Ronald N

, p. 3445 - 3451 (2002)

Porphyrin containing molecular building blocks have been linked together using s-tetrazine or 1,3-dipolar coupling protocols to yield bis-porphyrin cavities of defined shape and size which were evaluated by molecular modelling.

Swern oxidation of bicyclo[2.2.1]hept-5-ene-2,3-diol and its pyrazine-fused derivatives: An improved synthesis of bicyclo[2.2.1]hept-5-ene-2,3-dione and an unexpected ring-opening reaction

Kobayashi, Tomoshige,Kobayashi, Sayuri

, p. 1062 - 1067 (2000)

An improved synthesis of bicyclo[2.2.1]hept-5-ene-2,3-dione by Swern oxidation of bicyclo[2.2.1]hept-5-ene-2,3-diol, and an unexpected ring-opening reaction by the Swern oxidation of pyrazine-fused congeners are described.

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