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
SMILES
COC(OC)OC
InChI
InChIKey=PYOKUURKVVELLB-UHFFFAOYSA-N
InChI=1S/C4H10O3/c1-5-4(6-2)7-3/h4H,1-3H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Microwave-assisted synthesis of imidazoles: reaction of p-toluenesulfonylmethyl isocyanide and polymer-bound imines. | 2005 Aug 15 |
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| Ni(II) Tol-BINAP-catalyzed enantioselective orthoester alkylations of N-acylthiazolidinethiones. | 2005 Aug 3 |
|
| Controlled copper-mediated chlorination of phenol rings under mild conditions. | 2007 Jun 11 |
|
| Vinylogous Mukaiyama aldol reactions with 4-oxy-2-trimethylsilyloxypyrroles: relevance to castanospermine synthesis. | 2007 Nov 3 |
|
| Synthesis of (+)-cortistatin A. | 2008 Jun 11 |
Patents
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| Code System | Code | Type | Description | ||
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TRIMETHYL ORTHOFORMATE
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DTXSID7027122
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XAM28819YJ
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149-73-5
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147479
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205-745-7
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1006
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9005
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m8250
Created by
admin on Sat Dec 16 06:58:18 GMT 2023 , Edited by admin on Sat Dec 16 06:58:18 GMT 2023
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PRIMARY | Merck Index |
SUBSTANCE RECORD
