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7H-Pyrrolo[2,3-d]pyrimidine-4-carboxylic acid

CAS No.
1005206-17-6
Chemical Name:
7H-Pyrrolo[2,3-d]pyrimidine-4-carboxylic acid
Synonyms
7H-Pyrrolo[2,3-d]pyrimidi...;7H-Pyrrolo[2,3-d]pyrimidine-4-carboxylic acid
CBNumber:
CB12485572
Molecular Formula:
C7H5N3O2
Molecular Weight:
163.13
MDL Number:
MFCD13193623
MOL File:
1005206-17-6.mol
MSDS File:
SDS
Last updated:2026-05-27 23:19:04

7H-Pyrrolo[2,3-d]pyrimidine-4-carboxylic acid Properties

storage temp. Storage temp. -20°C
Appearance White to light yellow Solid
CAS DataBase Reference 1005206-17-6

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
HS Code  2933599590

7H-Pyrrolo[2,3-d]pyrimidine-4-carboxylic acid price More Price(40)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth FP167570 7H-Pyrrolo[2,3-d]pyrimidine-4-carboxylic acid 1005206-17-6 1g $259.6 2026-06-04 Buy
Biosynth FP167570 7H-Pyrrolo[2,3-d]pyrimidine-4-carboxylic acid 1005206-17-6 2g $389.4 2026-06-04 Buy
Biosynth FP167570 7H-Pyrrolo[2,3-d]pyrimidine-4-carboxylic acid 1005206-17-6 5g $713.9 2026-06-04 Buy
Biosynth FP167570 7H-Pyrrolo[2,3-d]pyrimidine-4-carboxylic acid 1005206-17-6 10g $1103.3 2026-06-04 Buy
ChemScene CS-0034294 7H-Pyrrolo[2,3-d]pyrimidine-4-carboxylic acid ≥98% 1005206-17-6 1g $77 2026-06-04 Buy
Product number Packaging Price Buy
FP167570 1g $259.6 Buy
FP167570 2g $389.4 Buy
FP167570 5g $713.9 Buy
FP167570 10g $1103.3 Buy
CS-0034294 1g $77 Buy

7H-Pyrrolo[2,3-d]pyrimidine-4-carboxylic acid Chemical Properties, Uses, Production

Synthesis

Methyl 7H-pyrrolo[2,3-d]pyrimidine-4-carboxylate

1095822-17-5

7H-Pyrrolo[2,3-d]pyrimidine-4-carboxylic acid

1005206-17-6

Synthesis of compound 1. A solution of lithium hydroxide (LiOH, 0.236 g, 10.2 mmol) in water (4 mL) was slowly added dropwise to a solution of methyl 7H-pyrrolo[2,3-d]pyrimidine-4-carboxylate (1.4 g, 7.9 mmol) in tetrahydrofuran (THF, 20 mL) at 0 °C. The reaction mixture was stirred at 0 °C for 1 hour. Subsequently, the reaction solution was acidified with concentrated hydrochloric acid to pH 2. THF was evaporated off under reduced pressure and the remaining aqueous solution was cooled to 0 °C. The reaction was purified by filtration. The precipitated white solid was collected by filtration and dried under vacuum to afford 7H-pyrrolo[2,3-d]pyrimidine-4-carboxylic acid (Compound 1, 1.1 g, 85% yield). The product was characterized by 1H NMR (200 MHz, DMSO-d6): δ= 12.80 (broad peak, 1H), 8.95 (single peak, 1H), 7.87 (double peak, J = 2.8 Hz, 1H), 6.96 (double peak, J = 2.8 Hz, 1H). The mass spectrum (MS) showed m/z 164 [M + H]+.

References

[1] Patent: US2009/5359, 2009, A1. Location in patent: Page/Page column 16

7H-Pyrrolo[2,3-d]pyrimidine-4-carboxylic acid Preparation Products And Raw materials

7H-Pyrrolo[2,3-d]pyrimidine-4-carboxylic acid Suppliers

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7H-Pyrrolo[2,3-d]pyrimidine-4-carboxylic acid Spectrum

7H-Pyrrolo[2,3-d]pyrimidine-4-carboxylic acid 7H-Pyrrolo[2,3-d]pyrimidi... 1005206-17-6 MFCD17015971 oldold