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Details

Stereochemistry ACHIRAL
Molecular Formula C4H10O3
Molecular Weight 106.1204
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Methyl orthoformate

SMILES

COC(OC)OC

InChI

InChIKey=PYOKUURKVVELLB-UHFFFAOYSA-N
InChI=1S/C4H10O3/c1-5-4(6-2)7-3/h4H,1-3H3

HIDE SMILES / InChI
Molecular Formula C4H10O3
Molecular Weight 106.1204
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
149124
PubMed

PubMed

TitleDatePubMed
Tetra-μ-acetato-κO:O'-bis-{[4-methyl-N-(4-methyl-phen-yl)pyridin-2-amine-κN]copper(II)}.
2010-08-11
Tetra-μ-acetato-κO:O'-bis-{[N-(4-chloro-phen-yl)-4-methyl-pyridin-2-amine-κN]copper(II)}.
2010-08-04
2-(2-Naphth-yl)-1,3-dioxane.
2010-01-30
Preparation of silane-coated TiO2 nanoparticles in supercritical CO2.
2009-10-15
Recent synthetic studies leading to structural revisions of marine natural products.
2009-07-13
Electroosmotic flow-based pump for liquid chromatography on a planar microchip.
2008-11-01
Synthesis of (+)-cortistatin A.
2008-06-11
Vinylogous Mukaiyama aldol reactions with 4-oxy-2-trimethylsilyloxypyrroles: relevance to castanospermine synthesis.
2007-11-03
Controlled copper-mediated chlorination of phenol rings under mild conditions.
2007-06-11
Novel synthesis of the ortho ester derivative of 4,5-epoxymorphinan.
2006-02-02
Microwave-assisted synthesis of imidazoles: reaction of p-toluenesulfonylmethyl isocyanide and polymer-bound imines.
2005-08-15
Ni(II) Tol-BINAP-catalyzed enantioselective orthoester alkylations of N-acylthiazolidinethiones.
2005-08-03
Bismuth compounds in organic synthesis. A one-pot synthesis of homoallyl ethers and homoallyl acetates from aldehydes catalyzed by bismuth triflate.
2005-03-18
4-(9-fluorenylmethyloxycarbonyl)phenylhydrazine (FmPH): a new chromophoric reagent for quantitative monitoring of solid-phase aldehydes(1-3).
2004-07-09
Preparation of resin-bound N-(alpha-methoxyalkyl)amides: an advantageous use of solid-phase chemistry for the handling of unstable precursors of the versatile N-acyliminium ions.
2001-06-01
Patents

Patents

04001454
1
04003919
1
04009187
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04026907
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04179505
1
04243806
3
04246021
1
04346023
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04657919
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04670462
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04705864
3
04708823
1
04714492
2
04719054
3
04720586
2
04722939
1
04778869
1
04906765
1
04956482
1
04977272
1
05055613
1
05061626
1
05086065
1
05093460
1
05130335
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05225584
2
05258477
1
05330900
1
05334576
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05338888
1
05399778
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05663414
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05932747
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06008219
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06090950
4
06194576
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06207836
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06214996
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06271403
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06297375
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06316482
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06372735
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06372774
1
06458844
1
06498170
1
06534524
2
06630472
1
06784304
1
06787535
2
06844342
1
06844366
2
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:39:21 GMT 2025
Edited
by admin
on Mon Mar 31 21:39:21 GMT 2025
Record UNII
XAM28819YJ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TRIMETHYL ORTHOFORMATE
HSDB  
Preferred Name English
Methyl orthoformate
Systematic Name English
TRIMETHYL ORTHOFORMATE [HSDB]
Common Name English
TRIMETHOXYMETHANE
Systematic Name English
METHOXYMETHYLAL
Systematic Name English
ORTHOFORMIC ACID METHYL ESTER
Systematic Name English
ORTHOFORMIC ACID, TRIMETHYL ESTER
Common Name English
NSC-147479
Code English
PERMA-FLO OF
Brand Name English
ORTHOFORMIC ACID TRIMETHYL ESTER [MI]
Common Name English
Code System Code Type Description
WIKIPEDIA
TRIMETHYL ORTHOFORMATE
Created by admin on Mon Mar 31 21:39:21 GMT 2025 , Edited by admin on Mon Mar 31 21:39:21 GMT 2025
PRIMARY
EPA CompTox
DTXSID7027122
Created by admin on Mon Mar 31 21:39:21 GMT 2025 , Edited by admin on Mon Mar 31 21:39:21 GMT 2025
PRIMARY
FDA UNII
XAM28819YJ
Created by admin on Mon Mar 31 21:39:21 GMT 2025 , Edited by admin on Mon Mar 31 21:39:21 GMT 2025
PRIMARY
CAS
149-73-5
Created by admin on Mon Mar 31 21:39:21 GMT 2025 , Edited by admin on Mon Mar 31 21:39:21 GMT 2025
PRIMARY
NSC
147479
Created by admin on Mon Mar 31 21:39:21 GMT 2025 , Edited by admin on Mon Mar 31 21:39:21 GMT 2025
PRIMARY
ECHA (EC/EINECS)
205-745-7
Created by admin on Mon Mar 31 21:39:21 GMT 2025 , Edited by admin on Mon Mar 31 21:39:21 GMT 2025
PRIMARY
HSDB
1006
Created by admin on Mon Mar 31 21:39:21 GMT 2025 , Edited by admin on Mon Mar 31 21:39:21 GMT 2025
PRIMARY
PUBCHEM
9005
Created by admin on Mon Mar 31 21:39:21 GMT 2025 , Edited by admin on Mon Mar 31 21:39:21 GMT 2025
PRIMARY
MERCK INDEX
m8250
Created by admin on Mon Mar 31 21:39:21 GMT 2025 , Edited by admin on Mon Mar 31 21:39:21 GMT 2025
PRIMARY Merck Index
NIH
NCATS
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