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507-47-1

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507-47-1 Usage

Physical state

Colorless liquid

Odor

Faint amine-like

Primary uses

a. Intermediate in the synthesis of pharmaceuticals
b. Intermediate in the synthesis of agricultural chemicals

Additional uses

a. Corrosion inhibitor in metalworking fluids
b. Stabilizer in the production of plastic and rubber

Hazardous nature

Yes

Potential health effects

a. Eye irritation
b. Skin irritation
c. Harmful if swallowed
d. Harmful if inhaled

Safety precautions

Handle and store with caution, following safety recommendations

Check Digit Verification of cas no

The CAS Registry Mumber 507-47-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 507-47:
(5*5)+(4*0)+(3*7)+(2*4)+(1*7)=61
61 % 10 = 1
So 507-47-1 is a valid CAS Registry Number.
InChI:InChI=1/C2H4Cl3NO/c3-2(4,5)1(6)7/h1,7H,6H2

507-47-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-amino-2,2,2-trichloroethanol

1.2 Other means of identification

Product number -
Other names Ethanol, 1-amino-2,2,2-trichloro-

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:507-47-1 SDS

507-47-1Relevant articles and documents

Synthesis of N-(2,2,2-trichloro-1-hydroxyethyl)aldimines and their derivatives

Firsova, Yu. N.,Engel,Lozinskaya,Sosonyuk,Proskurnina,Zefirov

, p. 76 - 82 (2015)

The preparative procedure for the synthesis of N-(2,2,2-trichloro-1-hydroxyethyl)aldimines from the corresponding aldehyde, chloral, and ammonium acetate was developed. Preparative silylation and acylation of their hydroxy groups were acomplished for the first time. The possibility to use the synthesized O-trimethylsilyl and O-acetyl derivatives as the synthetic equivalents of N-nonsubstituted imines in the reactions with cyclopropenone was investigated.

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