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51816-01-4

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51816-01-4 Usage

Physical state

Colorless liquid

Uses

a. Intermediate in the production of pharmaceuticals
b. Intermediate in the production of agrochemicals
c. Production of dyes
d. Production of perfumes
e. Production of other specialty chemicals

Reactivity

Highly reactive

Safety precautions

a. Strong irritant to the skin
b. Strong irritant to the eyes
c. Strong irritant to the respiratory system
d. Handle with care
e. Proper safety precautions should be taken when working with this compound

Check Digit Verification of cas no

The CAS Registry Mumber 51816-01-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,8,1 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51816-01:
(7*5)+(6*1)+(5*8)+(4*1)+(3*6)+(2*0)+(1*1)=104
104 % 10 = 4
So 51816-01-4 is a valid CAS Registry Number.

51816-01-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclobutane-1,1-dicarbonyl chloride

1.2 Other means of identification

Product number -
Other names 1,1-CYCLOBUTANEDICARBONYL DICHLORIDE

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:51816-01-4 SDS

51816-01-4Relevant articles and documents

Enantioselective Henry reaction catalyzed by a C2-symmetric bis(oxazoline)-Cu(OAc)2·H2O complex

Ginotra, Sandeep K.,Singh, Vinod K.

, p. 3932 - 3937 (2008/09/21)

A C2-symmetric diethyl iPr-bis(oxazoline)-Cu(OAc) 2·H2O was found to be an efficient catalyst for catalyzing an enantioselective Henry reaction between nitromethane and various aldehydes to provide β-hydroxy nit

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