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Indole-7-carboxaldehyde - 98%, high purity , CAS No.1074-88-0

COA

Grade & Purity:

≥98%

Cas Number: 1074-88-0
Molecular Weight: 145.16
Beilstein Registry Number: 1524960
MDL number: MFCD01318152
PubChem CID: 2734629
PubChem SID: 504761170

In stock

Item Number

I122940

Grouped product items
SKU	Size	Availability	Price
I122940-250mg	250mg	3	$33.90
I122940-1g	1g	3	$104.90
I122940-5g	5g	3	$495.90
I122940-25g	25g	2	$2,231.90
I122940-100g	100g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$8,033.90

Basic Description

Synonyms	indole-7-carbaldehyde \| AB08653 \| HY-W008013 \| Indole-7-carboxaldehyde, 97% \| AC-22444 \| Indole-7-carboxaldehyde \| FT-0621437 \| MFCD01318152 \| 7-indole carboxaldehyde \| CHEBI:151092 \| 7-Indolecarboxaldehyde \| 1H-indole-7-carbaldehyde \| AMY6754 \| SY007723
Specifications & Purity	≥98%
Shipped In	Normal
Product Description	Used in an efficient synthesis of fused pyrroloquinolinedicarboxylates from acetylenedicarboxylates and triphenylphosphine. 1.reactant for preparation of antiandrogens. 2.reactant for preparation of antiplatelet agent. 3.reactant for preparation of liver X receptor (LXR) agonists. 4.reactant for preparation of antagonists of the EP3 receptor for prostaglandin E2. 5.reactant for preparation of inhibitors of glycoprotein perforin. 6.reactant for preparation of potent antitubulin agents. 7.reactant for preparation of potential insulin receptor activators. 8.reactant for preparation of potential scaffolds for peptide mimetics. 9.reactant for preparation of 5-Hydroxytryptamine1D receptor antagonist. 10.reactant for preparation of indolocarbazole kinase

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Indoles and derivatives
    - Subclass Indoles

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Indoles and derivatives
Subclass	Indoles
Intermediate Tree Nodes	Not available
Direct Parent	Indoles
Alternative Parents	Aryl-aldehydes Benzenoids Vinylogous amides Pyrroles Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Indole - Aryl-aldehyde - Benzenoid - Pyrrole - Vinylogous amide - Heteroaromatic compound - Azacycle - Aldehyde - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as indoles. These are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

Pubchem Sid	504761170
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504761170
IUPAC Name	1H-indole-7-carbaldehyde
INCHI	InChI=1S/C9H7NO/c11-6-8-3-1-2-7-4-5-10-9(7)8/h1-6,10H
InChIKey	XQVZDADGTFJAFM-UHFFFAOYSA-N
Smiles	C1=CC2=C(C(=C1)C=O)NC=C2
Isomeric SMILES	C1=CC2=C(C(=C1)C=O)NC=C2
WGK Germany	3
Molecular Weight	145.16
Beilstein	1524960
Reaxy-Rn	1524960
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1524960&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

7 results found

Lot Number	Certificate Type	Date	Item
H2212344	Certificate of Analysis	May 14, 2024	I122940
H2212299	Certificate of Analysis	May 14, 2024	I122940
H2212306	Certificate of Analysis	May 14, 2024	I122940
H2212494	Certificate of Analysis	May 14, 2024	I122940
H2212495	Certificate of Analysis	May 14, 2024	I122940
I1424087	Certificate of Analysis	May 07, 2022	I122940
E1428003	Certificate of Analysis	May 07, 2022	I122940

Chemical and Physical Properties

Sensitivity	Air Sensitive;light sensitive
Melt Point(°C)	86-89°C
Molecular Weight	145.160 g/mol
XLogP3	2.300
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	1
Exact Mass	145.053 Da
Monoisotopic Mass	145.053 Da
Topological Polar Surface Area	32.900 Å²
Heavy Atom Count	11
Formal Charge	0
Complexity	158.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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