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911060-82-7

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911060-82-7 Usage

Molecular weight

125.17 g/mol

Physical state

Colorless liquid

Odor

Faint

Solubility

Soluble in water and polar organic solvents

Uses

a. Reagent in organic synthesis
b. Preparation of pharmaceuticals and agrochemicals
c. Building block for synthesis of nitrogen-containing compounds

Chemical reactivity

a. Nucleophilic substitution reactions
b. Addition reactions

Versatility

Useful and versatile compound in organic chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 911060-82-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,1,0,6 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 911060-82:
(8*9)+(7*1)+(6*1)+(5*0)+(4*6)+(3*0)+(2*8)+(1*2)=127
127 % 10 = 7
So 911060-82-7 is a valid CAS Registry Number.

911060-82-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(Hydroxymethyl)cyclopentanecarbonitrile

1.2 Other means of identification

Product number -
Other names 1-hydroxymethylcyclohexanecarboxylic acid ethyl ester

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:911060-82-7 SDS

911060-82-7Relevant articles and documents

Synthesis of Spirocyclic β- and γ-Sultams by One-Pot Reductive Cyclization of Cyanoalkylsulfonyl Fluorides

Stepannikova, Kateryna O.,Vashchenko, Bohdan V.,Grygorenko, Oleksandr O.,Gorichko, Marian V.,Cherepakha, Artem Yu.,Moroz, Yurii S.,Volovenko, Yulian M.,Zhersh, Serhii

, p. 6530 - 6540 (2020/05/25)

One-pot intramolecular cyclization of novel sp3-enriched cyanoalkylsulfonyl fluorides into spirocyclic β- or γ-sultams is disclosed. The method relies on nitrile group reduction followed by sulfonylation of amino group thus formed upon mild con

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