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184834-44-4

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184834-44-4 Usage

Physical state

Colorless, odorless, and viscous liquid

Uses

a. Plasticizer for polymers
b. Raw material for the synthesis of pharmaceuticals and agrochemicals
c. Production of coatings, adhesives, and sealants

Properties when added to polymers

a. Improved flexibility
b. Enhanced durability
c. Increased resistance to heat and chemicals

Safety precautions

a. Harmful if ingested
b. Harmful if inhaled
c. Harmful if in contact with the skin
d. Handle with care in a well-ventilated area
e. Use appropriate protective equipment

Check Digit Verification of cas no

The CAS Registry Mumber 184834-44-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,8,3 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 184834-44:
(8*1)+(7*8)+(6*4)+(5*8)+(4*3)+(3*4)+(2*4)+(1*4)=164
164 % 10 = 4
So 184834-44-4 is a valid CAS Registry Number.

184834-44-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-5-oxo-5-phenylmethoxy-3-phenylmethoxycarbonylpentanoate

1.2 Other means of identification

Product number -
Other names 1,2-dibenzyl citrate

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:184834-44-4 SDS

184834-44-4Relevant articles and documents

The preparation of L,L-aspartame citric amide

Katritzky, Alan R.,Fang, Yunfeng,Prakash, Indra

, p. 675 - 677 (2007/10/03)

Mono-substituted L,L-aspartame citric amide 1 was prepared via coupling L,L-α-BMAP 3 with 1,2-dibenzyl citrate 2 prepared from selective hydrolysis of tribenzyl citrate 5.

Synthesis and siderophore activity of vibrioferrin and one of its diastereomeric isomers

Takeuchi, Yasuo,Nagao, Yoshiyuki,Toma, Kyoko,Yoshikawa, Yumiko,Akiyama, Teruaki,Nishioka, Hiromi,Abe, Hitoshi,Harayama, Takashi,Yamamoto, Shigeo

, p. 1284 - 1287 (2007/10/03)

Total synthesis of vibrioferrin (1), a siderophore, was achieved via a chiral dibenzyl citrate obtained by optical resolution. The citrate moiety of vibrioferrin was determined to have the R configuration and one of the diastereomeric isomers (1b) of 1 did not exhibit siderophore activity.

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