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15687-18-0

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15687-18-0 Usage

Originator

Tredum,Heacutepatrol

Uses

2-(4-chlorophenyl)-4-methylpentane-2,4-diol is a pharmaceutical drug with analgesic, antipyretic, and antihistaminic properties and can be used for preventative or early treatment of inflammatory syndromes.

Manufacturing Process

2-(p-Chlorophenyl)-4-methylpentane-2,4-diol (M.P. 76.5°C) was synthesized and condensation of 2-(p-chlorophenyl)-3-hydroxybytiric acid ethyl ester with CH3 MgI in ether.

Therapeutic Function

Antidepressant, Tranquilizer

Check Digit Verification of cas no

The CAS Registry Mumber 15687-18-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,6,8 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15687-18:
(7*1)+(6*5)+(5*6)+(4*8)+(3*7)+(2*1)+(1*8)=130
130 % 10 = 0
So 15687-18-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H17ClO2/c1-11(2,14)8-12(3,15)9-4-6-10(13)7-5-9/h4-7,14-15H,8H2,1-3H3

15687-18-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-chlorophenyl)-4-methylpentane-2,4-diol

1.2 Other means of identification

Product number -
Other names Fempentadiol [INN-Spanish]

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:15687-18-0 SDS

15687-18-0Downstream Products

15687-18-0Relevant articles and documents

Triflimide: An Overlooked High-Performance Catalyst of the Mukaiyama Aldol Reaction of Silyl Ketene Acetals with Ketones

Bae, Han Yong,List, Benjamin

, p. 13767 - 13772 (2018/09/12)

The Mukaiyama aldol reaction is a widely applied carbon–carbon bond forming reaction. However, despite numerous well-established methods using aldehydes as acceptors, only few examples exist with ketones. Here we report a highly practical catalytic approach to this transformation, namely, the triflimide catalyzed Mukaiyama aldol reaction of silyl ketene acetals with ketones. This method exhibits a broad substrate scope, is very rapid, tolerates functionalized substrates, and requires only parts-per-million catalyst loadings with preparative scale reactions up to hundreds of grams in excellent purity (>99 %).

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