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2-(Methoxymethoxy)-1,3-propanediyl Dibenzoate, with the CAS number 110874-21-0, is a compound that is characterized as a brown oil. It is primarily utilized in the field of organic synthesis due to its unique chemical properties.

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  • 110874-21-0 Structure
  • Basic information

    1. Product Name: 2-(Methoxymethoxy)-1,3-propanediyl Dibenzoate
    2. Synonyms: 2-(Methoxymethoxy)-1,3-propanediol Dibenzoat;2-(Methoxymethoxy)-1,3-propanediyl Dibenzoate;2-(Methoxymethoxy)-1,3-propanediol Dibenzoate
    3. CAS NO:110874-21-0
    4. Molecular Formula: C19H20O6
    5. Molecular Weight: 344.36
    6. EINECS: N/A
    7. Product Categories: Aromatics Compounds;Aromatics
    8. Mol File: 110874-21-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 434.961°C at 760 mmHg
    3. Flash Point: 189.123°C
    4. Appearance: /
    5. Density: 1.193g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.545
    8. Storage Temp.: N/A
    9. Solubility: Chloroform, Dichloromethane, Ethyl Acetate
    10. CAS DataBase Reference: 2-(Methoxymethoxy)-1,3-propanediyl Dibenzoate(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-(Methoxymethoxy)-1,3-propanediyl Dibenzoate(110874-21-0)
    12. EPA Substance Registry System: 2-(Methoxymethoxy)-1,3-propanediyl Dibenzoate(110874-21-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 110874-21-0(Hazardous Substances Data)

110874-21-0 Usage

Uses

Used in Organic Synthesis:
2-(Methoxymethoxy)-1,3-propanediyl Dibenzoate is used as a synthetic intermediate for the creation of various organic compounds. Its chemical structure allows it to be a versatile building block in the synthesis of complex molecules, contributing to the development of new pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-(Methoxymethoxy)-1,3-propanediyl Dibenzoate is used as a key component in the development of novel drug candidates. Its unique structure can be exploited to design and synthesize new molecules with potential therapeutic applications, targeting a wide range of diseases and medical conditions.
Used in Agrochemical Industry:
2-(Methoxymethoxy)-1,3-propanediyl Dibenzoate also finds application in the agrochemical industry, where it is employed as a starting material for the synthesis of new pesticides, herbicides, and other crop protection agents. Its incorporation into these products can lead to improved efficacy, selectivity, and environmental safety.
Used in Specialty Chemicals:
In the specialty chemicals sector, 2-(Methoxymethoxy)-1,3-propanediyl Dibenzoate is used as a raw material for the production of various high-value chemicals. These can include additives for the plastics and polymer industry, dyes and pigments, and other performance-enhancing chemicals that cater to specific market needs.

Check Digit Verification of cas no

The CAS Registry Mumber 110874-21-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,8,7 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 110874-21:
(8*1)+(7*1)+(6*0)+(5*8)+(4*7)+(3*4)+(2*2)+(1*1)=100
100 % 10 = 0
So 110874-21-0 is a valid CAS Registry Number.
InChI:InChI=1/C19H20O6/c1-22-14-25-17(12-23-18(20)15-8-4-2-5-9-15)13-24-19(21)16-10-6-3-7-11-16/h2-11,17H,12-14H2,1H3

110874-21-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-benzoyloxy-2-(methoxymethoxy)propyl] benzoate

1.2 Other means of identification

Product number -
Other names 1,3-dibenzoyloxy-2-methoxymethyloxypropane

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:110874-21-0 SDS

110874-21-0Relevant articles and documents

Novel nucleoside analogues as effective antiviral agents for Zika virus infections

Bassetto, Marcella,Basso, Mattia,Brancale, Andrea,Bugert, Joachim J.,Cima, Cecilia M.,Friese, Daniela,Salerno, Martina,Schwarze, Frank

, (2020)

Previously considered a neglected flavivirus, Zika virus has recently emerged as a public health concern due to its ability to spread rapidly and cause severe neurological disorders, such as microcephaly in newborn babies from infected mothers, and Guilla

METHOD FOR PRODUCING 2-NITROIMIDAZOLE DERIVATIVE

-

Page/Page column 7, (2009/12/23)

Disclosed is a method for producing a 2-nitroimidazole derivative having an acyclic sugar chain in a side chain which is suitable for production of a derivative having a radioisotope. Specifically disclosed is a method for producing 1-(1- benzoyloxymethyl

An efficient synthesis of 2-[(4-amino-1,2-dihydro-2-oxo-1- pyrimidinyl)methoxy]-1,3-propanediyl-di-L-valinate an anti-cytomegalovirus agent

Ghali,Johnston,Beauchamp,Naseree,Scott,Flanagan,Rodriguez

, p. 1591 - 1600 (2007/10/02)

An efficient synthesis for large scale preparation of the titled compound, a prodrug for the anti-HCMV agent 1-[2-hydroxy-1- (hydroxymethyl)ethoxy)methyl]cytosine, 9, has been developed. The product of each step is easily purified by either distillation o

Effect of Acyclic Pyrimidines Related to 9-guanine on Herpesviruses

Beauchamp, Lilia M.,Serling, Barbara L.,Kelsey, John E.,Biron, Karen K.,Collins, Peter,et al.

, p. 144 - 149 (2007/10/02)

A series of pyrimidines related to the potent antiherpetic agent 9-guanine (1, BW B759U), all containing the same acyclic chain, have been synthesized.Some of the compounds were derivatives of the naturally occuring bases, cytosine, uracil, and thymine; others included compounds in which the 5-position of the cytosine and uracil moieties were substituted by bromo, iodo, fluoro, methyl, and amino groups.Other variations of the cytosine derivatives were the 5-aza, 2-mercapto, 4-methylamino, 4-dimethylamino, and isocytosine congeners.A 4-aminopyrimidine adduct was also made.Antiviral testing showed that 1-cytosine (18, BW A1117U) was equivalent to the guanine analogue in the potency against human cytomegalovirus and Epstein Barr virus.Other compounds in the series were largely inactive in antiviral screening against the herpesviruses.

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