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1003-29-8
1H-Pyrrole-2-carbaldehyde

Catalog#:1P0001Y8

CAS:1003-29-8

MDL:MFCD00005217

Molecular Formula:C5H5NO

Molecular Weight:95.0993

UN Number:

Haz Class:

Packing Group:

Synonyms: pyrrole-2-carbaldehyde; pyrrole-2-carboxaldehyde; Pyrrole-2-carbaldehyde; AB1001210; DB-030991; ST2408936; TC-020750; AM20070639; FT-0603764; FT-0660920; P1246; TL80073583; MFCD00005217 (98%); 2-Pyrrolylcarboxaldehyde; 03P298; A-4046; 82655-EP2281822A1; 82655-EP2298758A1; 82655-EP2298759A1; 82655-EP2305664A1; I11-0010; Q-101975; BRD-K20608729-001-01-9; F0001-2423; 2-Pyrrolaldehyde; Z1741970067; InChI=1/C5H5NO/c7-4-5-2-1-3-6-5/h1-4,6; 24771-28-6; 6719-03-5; C5H5NO; PYRROLO-2-CARBOXALDEHYDE; C5-H5-N-O; CID13854; Pyrrole-2-carboxaldehyde, 99% 5g; ACN-025641; 254729-95-8; M871; Pyrrole-2-carboxaldehyde, 98% - 5G 5g; C2404; C2519; A16168; alpha-Pyrrolaldehyde; 2-Pyrrolcarbaldehyde; Pyrrol-2-carboxaldehyde; 2-carboxaldehyde-1H-pyrrole; 1H-pyrrole-2-carboxyaldehyde; 1-Pyrrole-2-carboxaldehyde; 1H-Pyrrole-2-carbaldehyde; UNII-068TSM6S6P; MFCD00005217; pyrrole carboxaldehyde; CHEBI:59978; 2-Formyl-1H-pyrrole; 1H-Pyrrolecarboxaldehyde; NSC 66394; NSC 112885; 1(H)-pyrrole carboxaldehyde; 068TSM6S6P; PYRROLE-2-CARBOXALDEHYDE; Pyrrole-2-carboxaldehyde (8CI); ZSKGQVFRTSEPJT-UHFFFAOYSA-N; Pyrrole-2-carboxaldehyde, 99%; formyl-pyrrole; pyrrole aldehyde; 2-Formyl-pyrrole; pyrrol-2-aldehyde; 2-pyrrole aldehyde; EINECS 213-705-5; pyrrole-carboxaldehyde; 1003-29-8; 2-pyrrolcarboxaldehyde; PubChem9140; pyrrol-2-carbaldehyde; 2-pyrrole carbaldehyde; .alpha.-Pyrrolaldehyde; pyrrole 2-carboxaldehyde; AI3-35104; AC1Q6PVO; Epitope ID:136032; AC1L22MH; 2-Formylpyrrole; ACMC-1CF29; KSC174S1B; 1H-Pyrrole-2-carbaldehyde #; 1( H)-Pyrrole carboxaldehyde; Jsp000093; CHEMBL2229658; DTXSID3061392; Pyrrole-2-carboxaldehyde, 98%; CTK0H4910; ACT05084; 1H-Pyrrole-2-carboxaldehyde; BCP13856; CS-D0925; NSC66394; STR01055; ZINC1069171; ANW-14239; BBL022920; HTS027704; NSC-66394; NSC112885; Pyrrole-2-aldehyde; QC-480; RW1987; SBB004389; STK320567; AKOS000120434; AB00388; AC-4316; AS06197; CM13861; LS00119; 2-Pyrrolecarbaldehyde; MCULE-4586543663; Methanol, 1-(2H-pyrrol-2-ylidene)-; NSC-112885; PS-9355; RP00378; RTC-020750; TRA0018876; AJ-24848; AK-25235; AN-12118; 2-Pyrrolecarboxaldehyde; AN-29312; BC210794; BP-10720; BR-25235; CJ-04708; SC-00019; SC-29059; ST056382; SY001497; ZB015828;

Keywords: 1003-29-8,MFCD00005217,1P0001Y8,1H-Pyrrole-2-carbaldehyde,C5H5NO

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Catalog# Purity Size Price Dis. Price Availability Quantity
1P0001Y8 98% 5g $7.00 $5.00 In Stock USA ADD TO CART BUY NOW
1P0001Y8 98% 10g $9.00 $7.00 In Stock USA ADD TO CART BUY NOW
1P0001Y8 98% 25g $17.00 $13.00 In Stock USA ADD TO CART BUY NOW
1P0001Y8 98% 100g $64.00 $48.00 In Stock USA ADD TO CART BUY NOW
1P0001Y8 98% 500g $319.00 $240.00 In Stock USA ADD TO CART BUY NOW

  • 1H-Pyrrole-2-carbaldehyde is an organic compound that is particularly useful in chemical synthesis. It belongs to the family of pyrroles with an aldehyde functional group at the second position of the pyrrole ring. This specific structure lends it to several applications in the synthesis of various organic molecules. 
    
    In synthetic organic chemistry, 1H-Pyrrole-2-carbaldehyde serves as a valuable building block for the construction of more complex molecules. A significant use of this compound is in the preparation of porphyrin derivatives. Porphyrins are a group of heterocyclic macrocycle organic compounds, which are important because they form the core of several important biological compounds, such as heme - the molecule that allows blood to carry oxygen.
    
    Additionally, 1H-Pyrrole-2-carbaldehyde can participate in condensation reactions with various active methylene compounds to synthesize substituted pyrroles, which themselves are valuable compounds in medicinal chemistry and materials science. These substituted pyrroles can be further elaborated for use in dyes, pigments, pharmaceuticals, and polymers.
    
    The aldehyde group on the 1H-Pyrrole-2-carbaldehyde offers a reactive site for nucleophilic addition reactions. For instance, it can be used to form Schiff bases through the reaction with amines. Schiff bases derived from pyrrole aldehydes are preeminent intermediates for synthesizing a wide range of heterocyclic compounds. They are also used in coordination chemistry to synthesize metal complexes that can serve as catalysts or have electronic properties beneficial in creating functional materials.
    
    Moreover, 1H-Pyrrole-2-carbaldehyde is used in the synthesis of pyrrolopyrimidine compounds which display a range of biological activities and can serve as useful intermediates for the development of drugs.
    
    In summary, 1H-Pyrrole-2-carbaldehyde is an important intermediate in chemical synthesis due to its versatile reactivity profile, allowing for the synthesis of an array of biologically and industrially relevant chemical compounds.

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