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Merck

251887

Sigma-Aldrich

2,4-Dimethoxyphenyl isocyanate

97%

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100 μL
MXP 12,107.00

MXP 12,107.00


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Estimated to ship onFebruary 18, 2025


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100 μL
MXP 12,107.00

About This Item

Linear Formula:
(CH3O)2C6H3NCO
CAS Number:
Molecular Weight:
179.17
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

MXP 12,107.00


Availability

Estimated to ship onFebruary 18, 2025


To order products, please contact your local dealer.

Assay

97%

form

liquid

bp

140 °C/11 mmHg (lit.)

mp

30 °C (lit.)

functional group

isocyanate

SMILES string

COc1ccc(N=C=O)c(OC)c1

InChI

1S/C9H9NO3/c1-12-7-3-4-8(10-6-11)9(5-7)13-2/h3-5H,1-2H3

InChI key

WRAZHLRMDRTLOZ-UHFFFAOYSA-N

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This Item
SAB5700040HPA055748HPA062833
conjugate

unconjugated

conjugate

-

conjugate

unconjugated

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

product line

Prestige Antibodies® Powered by Atlas Antibodies

product line

-

product line

Prestige Antibodies® Powered by Atlas Antibodies

product line

Prestige Antibodies® Powered by Atlas Antibodies

UniProt accession no.

Q8WVQ1

UniProt accession no.

Q8WVQ1

UniProt accession no.

Q86VP6

UniProt accession no.

Q86VP6

species reactivity

human

species reactivity

human

species reactivity

human

species reactivity

human

Application

2,4-Dimethoxyphenyl isocyanate has been used in the preparation of pyrrolo[3,2-d]pyrimidines[1].

Pictograms

Health hazardExclamation mark

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Frederik J R Rombouts et al.
Journal of combinatorial chemistry, 7(4), 589-598 (2005-07-12)
The first solid-phase methodology for the preparation of pyrrolo[3,2-d]pyrimidines is presented. Merrifield resin bearing a cysteamine "traceless" linker was treated with 4-oxo-N-(PhF)proline benzyl ester (10; PhF = 9-(9-phenylfluorenyl)) to provide resin-bound aminopyrrole 20, which was treated with ethyl, phenyl, 4-phenoxyphenyl

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