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17931-56-5

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17931-56-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17931-56-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,3 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17931-56:
(7*1)+(6*7)+(5*9)+(4*3)+(3*1)+(2*5)+(1*6)=125
125 % 10 = 5
So 17931-56-5 is a valid CAS Registry Number.

17931-56-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl bicyclo[2.2.1]hept-2-ene-2,3-dicarboxylate

1.2 Other means of identification

Product number -
Other names Dimethyl Bicyclo<2.2.1>hept-2-ene-2,3-dicarboxylate

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:17931-56-5 SDS

17931-56-5Relevant articles and documents

THRB RECEPTOR AGONIST COMPOUND AND PREPARATION METHOD AND USE THEREOF

-

, (2020/07/07)

The present invention discloses a compound represented by the following Formula (I) and a pharmaceutically acceptable salt thereof. The compound improves the THRα selectivity while maintaining good THRβ agonistic activity, thereby improving properties of

BRIDGED RING COMPOUNDS AS HEPATITIS C VIRUS (HCV) INHIBITORS AND PHARMACEUTICAL APPLICATIONS THEREOF

-

, (2014/02/16)

Provided herein is a compound having Formula (I), or a stereoisomer, a geometric isomer, a tautomer, an N-oxide, a hydrate, a solvate, a metabolite, a pharmaceutically acceptable salt or a prodrug thereof, which can be used for treating HCV infection or a HCV disorder. Also provided herein are pharmaceutical compositions comprising the compounds disclosed herein, which can be used for treating HCV infection or a HCV disorder.

Regioselective Catalytic Transfer Hydrogenation of Dimethyl Bicyclohepta-2,5-diene-2,3-dicarboxylate, Dimethyl Bicyclohept-2-ene-2,3-dicarboxylate, and Related Compounds over Palladium on Carbon

Tabor, Derrick C.,White, Franklin H.,Collier, L. Warren,Evans, Slayton A.

, p. 1638 - 1643 (2007/10/02)

The catalytic transfer hydrogenation (CTH) of dimethyl bicyclohepta-2,5-diene-2,3-dicarboxylate (3) on palladium on carbon is highly regioselective, giving predominant reduction at the least-substituted olefinic site.The CTH of dimethyl bicyclohept-2-ene-2,3-dicarboxylate also occurs with exclusive suprafacial exo addition of hydrogen to afford the endo isomer.An increase in the relative concentration of palladium on carbon (ca. 40-45 wt/wt percent based on the acceptor) accelerates the rate of CTH while the substituted cyclohexenes undergo CTH faster than cyclohexene with dimethyl bicyclohept-2-ene-2,3-dicarboxylate.

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