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Thiocyanic acid 3-methylbutyl ester, also known as 3-methylbutyl thiocyanate, is an organic compound with the chemical formula C6H11NS. It is a colorless liquid with a pungent odor and is derived from the esterification of thiocyanic acid and 3-methylbutanol. Thiocyanic acid 3-methylbutyl ester is used as a flavoring agent and fragrance component in various industrial applications, such as food, beverages, and cosmetics. It is also employed in the synthesis of other chemicals and pharmaceuticals. Due to its potential irritant properties, it is essential to handle Thiocyanic acid 3-methylbutyl ester with care and follow proper safety guidelines.

543-50-0

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543-50-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 543-50-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,4 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 543-50:
(5*5)+(4*4)+(3*3)+(2*5)+(1*0)=60
60 % 10 = 0
So 543-50-0 is a valid CAS Registry Number.

543-50-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name isopentylsulfanyl cyanate

1.2 Other means of identification

Product number -
Other names Isopentylrhodanid

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:543-50-0 SDS

543-50-0Relevant academic research and scientific papers

A new synthesis of alkane and polyfluoroalkanesulfonyl chlorides

Benfodda, Zohra,Guillen, Franck,Arnion, Helene,Dahmani, Abdelkader,Blancou, Hubert

experimental part, p. 355 - 361 (2010/07/16)

This study describes a new and advantageous procedure for the synthesis of alkanesulfonyl chlorides (2) by the reaction of alkyl thiocyanates (1) with sulfuryl chloride in a mixture of acetic acid and water. The alkanesulfonyl chlorides were obtained in good yields.

Aminoalcohol derivatives

-

Page/Page column 13, (2010/02/12)

The present invention relates to a compound formula[I]: wherein X is bond, —CH2—, —O— or —NH—, R1 and R12 are each independently hydrogen, halogen, lower alkyl, etc., R2 is hydrogen or optionally substituted lower alkyl, R3 is hydrogen or an amino protective group, R4, R5 and R6 are each independently hydrogen or optionally substituted lower alkyl, R7 is -Z-R13, in which Z is bond, etc., and R13 is carboxy, lower alkoxycarbonyl, (lower alkylsulfonyl)carbamoyl or lower alkanoylsulfamoyl, R8 is —Y—R9, in which Y is bond, —CH2—, —O—, —S—, etc., and R9 is hydrogen, lower alkyl, cyclo(lower)alkyl, etc., and R11 is hydrogen, lower alkyl, lower alkoxy, etc., or a salt thereof. The compound [I] of the present invention and pharmaceutically acceptable salts thereof are useful for the prophylactic and/or the therapeutic treatment of pollakiurea or urinary incontinence.

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