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349674

Sigma-Aldrich

Dimethyl cis-1,2,3,6-tetrahydrophthalate

99%

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10 G
$242.00

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10 G
$242.00

About This Item

Empirical Formula (Hill Notation):
C10H14O4
CAS Number:
4841-84-3
Molecular Weight:
198.22
MDL number:
MFCD00209581
UNSPSC Code:
12352100
PubChem Substance ID:
24861699
NACRES:
NA.22

$242.00

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Quality Level

100

Assay

99%

form

liquid

refractive index

n20/D 1.472 (lit.)

bp

141-142 °C/20 mmHg (lit.)

density

1.145 g/mL at 25 °C (lit.)

functional group

ester

SMILES string

COC(=O)[C@H]1CC=CC[C@H]1C(=O)OC

InChI

1S/C10H14O4/c1-13-9(11)7-5-3-4-6-8(7)10(12)14-2/h3-4,7-8H,5-6H2,1-2H3/t7-,8+

InChI key

DVVAGRMJGUQHLI-OCAPTIKFSA-N

Related Categories

General description

Epoxidation of dimethyl cis-1,2,3,6-tetrahydrophthalate has been reported.[1] Desymmetrization of dimethyl cis-1,2,3,6-tetrahydrophthalate to (1S,2R)-1-methyl-cis-1,2,3,6-tetra-hydrophthalate has been reported.[2]

Application

Dimethyl cis-1,2,3,6-tetrahydrophthalate may be used in chemical synthesis.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBH7443
S36955
07520TC
23022EA
09528BA

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Stereospecific epoxidation of dihydrophthalates.
Cerefice SA and Fields EK.
The Journal of Organic Chemistry, 41(2), 355-361 (1976)
The use of enzymes in organic synthesis and the life sciences: perspectives from the Swiss Industrial Biocatalysis Consortium (SIBC).
Meyer H-P, et al.
Catalysis Science & Technology, 3(1), 29-40 (2013)

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