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MilliporeSigma

515574

Sigma-Aldrich

Isoindoline

97%

Synonym(s):

1,3-Dihydro-2H-isoindole, 1,3-Dihydroisoindole, 2,3-Dihydro-1H-isoindole, 2-Azaindan

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About This Item

Empirical Formula (Hill Notation):
C8H9N
CAS Number:
496-12-8
Molecular Weight:
119.16
MDL number:
MFCD00605324
UNSPSC Code:
12352100
PubChem Substance ID:
24873832
NACRES:
NA.22

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Quality Level

100

assay

97%

refractive index

n20/D 1.57 (lit.)

bp

221 °C (lit.)

mp

17 °C (lit.)

density

1.05 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

C1NCc2ccccc12

InChI

1S/C8H9N/c1-2-4-8-6-9-5-7(8)3-1/h1-4,9H,5-6H2

InChI key

GWVMLCQWXVFZCN-UHFFFAOYSA-N

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320536AG962AG912
Isoindoline 97%

Sigma-Aldrich

515574

Isoindoline

Thionyl chloride reagent grade, 97%

Sigma-Aldrich

320536

Thionyl chloride

β Amyloid 1-40, aβ, ultra pure, HFIP, recombinant human

Sigma-Aldrich

AG962

β Amyloid 1-40, aβ, ultra pure, HFIP, recombinant human

β Amyloid 1-42, aβ, ultra pure, TFA, recombinant human

Sigma-Aldrich

AG912

β Amyloid 1-42, aβ, ultra pure, TFA, recombinant human

assay

97%

assay

97%

assay

>97%

assay

>97%

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

density

1.05 g/mL at 25 °C (lit.)

density

1.631 g/mL at 25 °C (lit.)

density

-

density

-

bp

221 °C (lit.)

bp

79 °C (lit.)

bp

-

bp

-

mp

17 °C (lit.)

mp

−105 °C (lit.)

mp

-

mp

-

storage temp.

2-8°C

storage temp.

-

storage temp.

-

storage temp.

-

Application

Used to make a chiral diamine catalyst from L-proline for the asymmetric acylation of alcohols.[1]

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

No data available

flash_point_c

No data available

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
SHBK9083
SHBH1270V
SHBD1511V
SHBB2521V
43796TMV

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Organic Syntheses, 83, 70-70 (2006)
Teresa Mancilla-Percino et al.
Archiv der Pharmazie, 349(3), 175-185 (2016-01-15)
IC50 values were obtained for two series of isoindolines derived from α-amino acids over cyclooxygenase 1 and 2 (COX-1 and COX-2). In order to explain the biological activity observed, a structure-activity relationship (SAR) model was achieved for the tested compounds
Yulia Kaluzhny et al.
Alternatives to laboratory animals : ATLA, 43(2), 101-127 (2015-05-23)
The 7th Amendment to the EU Cosmetics Directive and the EU REACH Regulation have reinforced the need for in vitro ocular test methods. Validated in vitro ocular toxicity tests that can predict the human response to chemicals, cosmetics and other

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