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1950-68-1

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1950-68-1 Usage

Description

4-Methoxybenzenesulfonyl hydrazide is a chemical compound with the chemical formula C7H10N2O3S. It is primarily used in the industry as a blowing agent, which is a substance that helps generate a gas to produce foam in a polymer matrix. 4-METHOXYBENZENESULFONYL HYDRAZIDE is known for its high gas yields and excellent storage stability.

Uses

Used in Rubber and Plastics Industry:
4-Methoxybenzenesulfonyl hydrazide is used as a blowing agent for the production of foam in various types of rubber and plastics. Its ability to generate high gas yields and maintain excellent storage stability makes it a valuable component in the manufacturing process.
Safety Precautions:
It is important to handle 4-Methoxybenzenesulfonyl hydrazide with care, as it can cause skin and eye irritation, as well as respiratory irritation upon inhalation. Additionally, it is harmful if swallowed. Proper safety measures should be taken to minimize exposure and ensure the safe use of this chemical compound in industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1950-68-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,5 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1950-68:
(6*1)+(5*9)+(4*5)+(3*0)+(2*6)+(1*8)=91
91 % 10 = 1
So 1950-68-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H10N2O3S/c1-12-6-2-4-7(5-3-6)13(10,11)9-8/h2-5,9H,8H2,1H3

1950-68-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methoxybenzenesulfonohydrazide

1.2 Other means of identification

Product number -
Other names p-methoxybenzenesulfonylhydrazine

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:1950-68-1 SDS

1950-68-1Relevant articles and documents

DOCK1-INHIBITING COMPOUND AND USE THEREOF

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Paragraph 0156; 0157, (2021/10/07)

Provided is a compound that is usable as an active ingredient of an anticancer agent. Preferably provided is a compound that has DOCK1-inhibiting activity and exerts an anticancer effect based on the activity. A compound represented by the following formula (A) or a salt thereof: wherein X represents a carbon atom or a nitrogen atom; Y represents an oxygen atom, a hydroxy group, or a hydrocarbon group; R1 and R2 are different, and each represents a hydrogen atom or a group represented by the following formula (A-1): (wherein R6 represents a pyrrolidino group or a phenyl group, and n2 is 0 or 1) ; R3 represents -CO-R7 (wherein R7 is an alkoxy group, an alkyl group, or an alkylamino group), a 1,3-oxazole group, an alkylhydroxy group, a hydrogen atom, or an oxygen atom; R4 represents a hydrogen atom, an oxygen atom, or a hydrocarbon group in which one or more hydrogen atoms may be replaced by one or more substituents; R5 represents a halogen atom, a halogenated alkyl group, or a halogenated alkylthio group; and n1 is an integer of 0 to 5; and

5-HT2A AGONISTS FOR USE IN TREATMENT OF DEPRESSION

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Paragraph 0435-0436, (2021/05/14)

The present invention relates to agonists of the 5-HT2A serotonin receptors and their medical uses. In one aspect the invention relates to 5-HT2A agonists of formula (I). In second aspect, the invention relates to selective 5-HT2A agonists of formula (II). In another aspect, the invention relates to mixed 5-HT2A/5-HT2C agonists of formula (III). In yet another aspect, the invention relates to 5-HT2A agonists for use in the treatment of a depressive disorder, more particular a 5-HT2A agonist for the use in the treatment of treatment-resistant depression.

Palladium-Catalyzed Direct C-H Arylation of 3-Butenoic Acid Derivatives

Yang, Shan,Liu, Lingling,Zhou, Zheng,Huang, Zhibin,Zhao, Yingsheng

supporting information, p. 296 - 299 (2021/01/13)

We report herein a direct method to synthesize 4-aryl-3-butenoic acid through a carboxylic-acid-directed oxidative Heck reaction. The various 4-aryl-3-butenoic acids are easily prepared in moderate to good yields. In view of the promising bioactivity of 4-phenyl-3-butenoic acid previously reported, its derivatives reported here may be bioactive.

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