What is the 1H-Imidazole-4-carbaldehyde?

1H-Imidazole-4-carbaldehyde is White to light yellow powder, while it's Molecular Formula is C4H4N2O. White to light yellow powder Imidazole-4-carboxaldehyde is a 4-formyl derivative of imidazole used in the preparation of C17,20-lyase inhibitor for the treatment of androgen-dependent prostate cancer. It is also used in the synthesis of other biologically active compounds such as antimalarial drugs, fabrication of colorimetric chemosensor.

What is the CAS number for 1H-Imidazole-4-carbaldehyde?

The CAS number of 1H-Imidazole-4-carbaldehyde is 3034-50-2.

What is 1H-Imidazole-4-carbaldehyde (3034-50-2) used for?

1H-Imidazole-4-carbaldehyde, also known as 4-Imidazolecarboxaldehyde, is a 4-formyl derivative of imidazole, which is a heterocyclic organic compound. It is characterized by its white to light yellow powder appearance and is known for its role in the synthesis of various biologically active compounds.InChI:InChI=1/C5H6N2O/c1-4(8)5-2-6-3-7-5/h2-3H,1H3,(H,6,7)

What is the 1H-Imidazole-4-carbaldehyde?

1H-Imidazole-4-carbaldehyde is White to light yellow powder, while it's Molecular Formula is C4H4N2O. White to light yellow powder Imidazole-4-carboxaldehyde is a 4-formyl derivative of imidazole used in the preparation of C17,20-lyase inhibitor for the treatment of androgen-dependent prostate cancer. It is also used in the synthesis of other biologically active compounds such as antimalarial drugs, fabrication of colorimetric chemosensor.

What is the CAS number for 1H-Imidazole-4-carbaldehyde?

The CAS number of 1H-Imidazole-4-carbaldehyde is 3034-50-2.

What is 1H-Imidazole-4-carbaldehyde (3034-50-2) used for?

1H-Imidazole-4-carbaldehyde, also known as 4-Imidazolecarboxaldehyde, is a 4-formyl derivative of imidazole, which is a heterocyclic organic compound. It is characterized by its white to light yellow powder appearance and is known for its role in the synthesis of various biologically active compounds.InChI:InChI=1/C5H6N2O/c1-4(8)5-2-6-3-7-5/h2-3H,1H3,(H,6,7)

3034-50-2

Product Name1H-Imidazole-4-carbaldehyde
Molecular FormulaC₄H₄N₂O
Molecular Weight96.0886
Purity99%
AppearanceWhite to light yellow powder

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Product Details

Quick Details

CasNo： 3034-50-2
Molecular Formula： C₄H₄N₂O
Appearance： White to light yellow powder
Purity： 99%

Manufacturers supply cost-effective and customizable 1H-Imidazole-4-carbaldehyde 3034-50-2

Molecular Formula:C4H4N2O
Molecular Weight:96.0886
Appearance/Colour:White to light yellow powder
Vapor Pressure:0mmHg at 25°C
Melting Point:174-177 °C(lit.)
Refractive Index:1.535
Boiling Point:367.8 °C at 760 mmHg
PKA:11.05±0.10(Predicted)
Flash Point:179.8 °C
PSA：45.75000
Density:1.322 g/cm³
LogP:0.22220

1H-Imidazole-4-carbaldehyde(Cas 3034-50-2) Usage

General Description

1H-Imidazole-4-carbaldehyde is a versatile intermediate in organic synthesis, accessible through various methods such as regioselective N-alkylation of 4-formylimidazole, photooxidative cleavage of urocanic acid, and efficient synthetic routes involving lithiation and formylation. Its reactivity and applications are highlighted by its role in selective alkylation reactions, photochemical transformations, and as a precursor for N-protected derivatives.

InChI:InChI=1/C5H6N2O/c1-4(8)5-2-6-3-7-5/h2-3H,1H3,(H,6,7)

3034-50-2 Relevant articles

Regioselective n-alkylation of 4-formylimidazole

Su, Qiaogong,Wood, Jeffery L.

, p. 3383 - 3389 (2000)

We describe here a high yield and highly...

Urocanic acid photobiology. Purine-assisted photooxidation to 1H- imidazole-4(5)-carboxaldehyde

Mohammad,Kasper,Morrison

, p. 4903 - 4906 (1994)

Urocanic acid undergoes photooxidative c...

A simple and efficient synthesis of N-protected imidazole-4-carbaldehyde

Winter,Retey

, p. 245 - 246 (1994)

Successive addition of BuLi, triethylsil...

-

Brocklehurst,Griffiths

, p. 2407 (1968)

Method for preparing 1H-imidazole-4-carbonitrile

-

Paragraph 0034; 0043-0049, (2019/02/26)

The invention discloses a method for pre...

Synthesis method of 1H-imidazole-4-carboxylic acid

-

Paragraph 0021; 0028; 0035; 0042; 0049, (2018/05/16)

The invention discloses a synthesis meth...

Hydrazinyl-Substituted Heteroaryl Compounds and Methods for Producing a Conjugate

-

Paragraph 0540-0542, (2017/09/29)

The present disclosure provides conjugat...

Halogen–metal exchange on bromoheterocyclics with substituents containing an acidic proton via formation of a magnesium intermediate

Tian, Qingqiang,Shang, Suqin,Wang, Huajun,Shi, Guoqiang,Li, Zhiyao,Yuan, Jianyong

supporting information, (2017/12/05)

A selective and practical bromine–metal ...

3034-50-2 Process route

: 3465-72-3
urocanic Acid

: 645-65-8
2-(1H-imidazol-4-yl)acetic acid

: 3034-50-2
4⁽⁵⁾formylimidazole

: 1072-84-0
imidazole-4-carboxylic acid

Conditions

Conditions	Yield
With dihydrogen peroxide; pH=7.2; Product distribution / selectivity; aqueous phosphate buffer;
With dihydrogen peroxide; In water; pH=7.2; Product distribution / selectivity;

: 3465-72-3
urocanic Acid

: 645-65-8
2-(1H-imidazol-4-yl)acetic acid

: 3034-50-2
4⁽⁵⁾formylimidazole

: 1072-84-0
imidazole-4-carboxylic acid

: 7699-35-6
(Z)-urocanic acid

Conditions

Conditions	Yield
With dihydrogen peroxide; pH=7.2; Product distribution / selectivity; aqueous phosphate buffer; UV-irradiation;

3034-50-2 Upstream products

822-55-9
(1H-imidazol-4-yl)methanol
822-55-9
1H-imidazole-5-methanol
1025907-10-1
1-(N,N-dimethylsulfamoyl)-2-(triethylsilyl)imidazole-4-carbaldehyde
33016-47-6
(1-tritylimidazol-4-yl)carboxaldehyde

3034-50-2 Downstream products

3465-72-3
urocanic Acid
39021-62-0
1-methylimidazole-5-carbaldehyde
67565-89-3
5-methyl-3-phenyl-isoxazole-4-carboxylic acid (1⁽³⁾H-imidazol-4-ylmethylene)-hydrazide
108320-28-1
8-(4-Methylphenylsulfonyl)-5H-imidazo<1,5-a>azepin

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