92050-02-7

Basic information

• Product Name: 2,6-DIISOPROPYLPHENYL SULFAMATE
• Synonyms: 2,6-DIISOPROPYLPHENYL SULFAMATE;sulfaMate de diisopropyl-2,6 phenyle
• CAS NO: 92050-02-7
• Molecular Formula: C₁₂H₁₉NO₃S
• Molecular Weight: 0
• Mol File: 92050-02-7.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,6-DIISOPROPYLPHENYL SULFAMATE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-DIISOPROPYLPHENYL SULFAMATE(92050-02-7)
• EPA Substance Registry System: 2,6-DIISOPROPYLPHENYL SULFAMATE(92050-02-7)

Safety Data

• Hazardous Substances Data: 92050-02-7(Hazardous Substances Data)

Usage

General Description

2,6-DIISOPROPYLPHENYL SULFAMATE is a chemical compound with the molecular formula C13H21NO3S. It is a sulfamate ester and is commonly used as a plasticizer in various industrial applications, particularly in the production of polyvinyl chloride (PVC) products. It acts as a non-phthalate alternative to traditional plasticizers and is known for its strong plasticizing effect, low volatility, and high thermal stability. Additionally, 2,6-DIISOPROPYLPHENYL SULFAMATE is also used as an anti-scaling agent in water treatment processes. It is important to handle this chemical with care due to its potential hazards if not used properly.

Upstream product

• 2078-54-8 2,6-diisopropylphenol 
• 73748-46-6 <2,6-bis(1-methylethyl)phenoxy>sulfonyl isocyanate 

Downstream Products

• 1026007-06-6 Sulfamic acid[[2,6-bis(1-methylethyl)phenyl]acetyl]-2,6-bis(1-methyl-ethyl)phenyl ester 
• 867262-98-4 2,6-diisopropylphenyl {[1-(2-methoxyphenyl)-4-(3-methoxyphenyl)piperidin-4-yl]carbonyl}sulfamate 
• 1224432-13-6 2,6-diisopropylphenyl {[1-(diphenylmethyl)-4-(3-methoxyphenyl)-piperidin-4-yl]carbonyl}sulfamate 
• 166518-60-1 avasimibe 

Relevant articles and documents

Preparation of Sulfamates and Sulfamides Using a Selective Sulfamoylation Agent

Sulfamates and sulfamides are prevalent in biological molecules, but their universal synthetic methods are limited. We herein report a sulfamoylation agent with high solubility and shelf stability. Various sulfamates and sulfamides can be synthesized directly from alcohols or amines by employing this agent with high selectivity and high yields. This protocol was also successfully used for late-stage sulfamoylation of pharmaceuticals containing a hydroxyl or amino group.

NOVEL SULFONAMIDE DERIVATIVE

A compound of the formula (1): wherein m, n and p is independently an integer of 0 to 4 with the proviso that 3 a?| m + n a?| 8; X is the formula: NR4, etc.; R1, R3 and R4 are a substituted or unsubstituted aryl group, etc.; R2 is a hydrogen atom, etc.; a, b, c, d, e and f are a hydrogen atom or a substituted or unsubstituted alkyl group, etc.; Y is the formula: -SO2-, etc.; and Z is an oxygen atom, etc.; or a prodrug thereof or a pharmaceutically acceptable salt of the same has an activity of potentiating an expression of a low density lipoprotein receptor and thus is useful as an agent for treating hyperlipidemia or arteriosclerosis.