- Preparation of phenylheteroarylpiperidinamine derivatives for use as dipeptidyl peptidase-IV inhibitors, World Intellectual Property Organization, , ,
Cas no 945217-56-1 (3-methyl-1H,4H,5H,6H-pyrrolo[3,4-c]pyrazole)
945217-56-1 structure
Product Name:3-methyl-1H,4H,5H,6H-pyrrolo[3,4-c]pyrazole
CAS No:945217-56-1
MF:C6H9N3
MW:123.155760526657
MDL:MFCD16658458
CID:823608
PubChem ID:55287365
Update Time:2024-10-25
3-methyl-1H,4H,5H,6H-pyrrolo[3,4-c]pyrazole Chemical and Physical Properties
Names and Identifiers
-
- 3-Methyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole
- 1,4,5,6-tetrahydro-3-methyl-Pyrrolo[3,4-c]pyrazole
- 3-Methyl-1,4,5,6-tetrahydro-pyrrolo[3,4-c]pyrazole
- 3-methyl-2,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole
- 1,4,5,6-Tetrahydro-3-methylpyrrolo[3,4-c]pyrazole (ACI)
- 3-Methyl-1H,4H,5H,6H-pyrrolo[3,4-c]pyrazole
- 945217-56-1
- VMB21756
- CS-0053873
- MFCD16658458
- DA-19474
- SCHEMBL1705256
- SCHEMBL17162823
- DTXSID10717495
- PB18158
- AKOS006356870
- 3-methyl-1H,4H,5H,6H-pyrrolo[3,4-c]pyrazole
-
- MDL: MFCD16658458
- Inchi: 1S/C6H9N3/c1-4-5-2-7-3-6(5)9-8-4/h7H,2-3H2,1H3,(H,8,9)
- InChI Key: BRIYFUKTRQTBLR-UHFFFAOYSA-N
- SMILES: N1=C(C)C2CNCC=2N1
Computed Properties
- Exact Mass: 123.079647300g/mol
- Monoisotopic Mass: 123.079647300g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 9
- Rotatable Bond Count: 0
- Complexity: 115
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: -0.4
- Topological Polar Surface Area: 40.7?2
3-methyl-1H,4H,5H,6H-pyrrolo[3,4-c]pyrazole Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A049003136-250mg |
3-Methyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole |
945217-56-1 | 95% | 250mg |
$400.68 | 2023-08-31 | |
| Alichem | A049003136-1g |
3-Methyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole |
945217-56-1 | 95% | 1g |
$899.19 | 2023-08-31 | |
| Chemenu | CM188632-100mg |
3-Methyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole |
945217-56-1 | 95+% | 100mg |
$900 | 2021-08-05 | |
| Chemenu | CM188632-250mg |
3-Methyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole |
945217-56-1 | 95+% | 250mg |
$1155 | 2021-08-05 | |
| Chemenu | CM188632-1g |
3-Methyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole |
945217-56-1 | 95+% | 1g |
$2248 | 2021-08-05 | |
| CHENG DOU FEI BO YI YAO Technology Co., Ltd. | ARK-0695-5g |
3-METHYL-1,4,5,6-TETRAHYDROPYRROLO[3,4-C]PYRAZOLE |
945217-56-1 | 95% | 5g |
$1950 | 2023-09-07 | |
| Fluorochem | 223744-250mg |
3-Methyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole |
945217-56-1 | 95% | 250mg |
£418.00 | 2022-02-28 | |
| Fluorochem | 223744-1g |
3-Methyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole |
945217-56-1 | 95% | 1g |
£1043.00 | 2022-02-28 | |
| Chemenu | CM188632-1g |
3-Methyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole |
945217-56-1 | 95%+ | 1g |
$911 | 2024-07-19 | |
| eNovation Chemicals LLC | D683739-1g |
3-methyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole |
945217-56-1 | 95% | 1g |
$595 | 2024-05-24 |
3-methyl-1H,4H,5H,6H-pyrrolo[3,4-c]pyrazole Production Method
Production Method 1
Reaction Conditions
1.1 Reagents: Hydrochloric acid Solvents: Water ; 1.5 h, rt
Reference
Production Method 2
Reaction Conditions
Reference
- Heterocyclic compounds as dipeptidyl peptidase-iv inhibitors for the treatment or prevention of diabetes, United States, , ,
Production Method 3
Reaction Conditions
1.1 Reagents: Hydrochloric acid Solvents: Ethanol , Water ; 3 h, 90 °C
Reference
- Preparation of substituted six-membered heterocyclic amine compounds as DPP-IV inhibitors, China, , ,
Production Method 4
Reaction Conditions
1.1 Reagents: Hydrochloric acid Solvents: Methanol ; 12 h, rt
1.2 Reagents: Ammonium hydroxide , Ammonia Solvents: Methanol , Water
1.2 Reagents: Ammonium hydroxide , Ammonia Solvents: Methanol , Water
Reference
- Aminotetrahydropyrans as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetes, hyperglycemia, and obesity, United States, , ,
Production Method 5
Reaction Conditions
1.1 Reagents: Hydrochloric acid Solvents: Water ; 1.5 h, rt
Reference
- Preparation of pyrrolopyrazolylaminocyclohexanes and related compounds as dipeptidylpeptidase-IV (DPP-IV) inhibitors for the treatment or prevention of diabetes, World Intellectual Property Organization, , ,
3-methyl-1H,4H,5H,6H-pyrrolo[3,4-c]pyrazole Raw materials
- 1,1-Dimethylethyl 2,6-dihydro-3-methyl-2-[[2-(trimethylsilyl)ethoxy]methyl]pyrrolo[3,4-c]pyrazole-5(4H)-carboxylate
- tert-butyl 3-methyl-1H,4H,5H,6H-pyrrolo[3,4-c]pyrazole-5-carboxylate
3-methyl-1H,4H,5H,6H-pyrrolo[3,4-c]pyrazole Preparation Products
3-methyl-1H,4H,5H,6H-pyrrolo[3,4-c]pyrazole Related Literature
-
Qiaoe Wang,Meiling Lian,Xiaowen Zhu,Xu Chen RSC Adv., 2021,11, 192-197
-
Nan Fu,Naphaporn Chiewchan,Xiao Dong Chen Food Funct., 2020,11, 211-220
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Amandine Altmayer-Henzien,Valérie Declerck,David J. Aitken,Ewen Lescop,Denis Merlet,Jonathan Farjon Org. Biomol. Chem., 2013,11, 7611-7615
-
Albertus D. Handoko,Khoong Hong Khoo,Teck Leong Tan,Hongmei Jin,Zhi Wei Seh J. Mater. Chem. A, 2018,6, 21885-21890
-
Xiaotong Feng,Lei Bian,Jie Ma,Lei Zhou,Xiayan Wang,Guangsheng Guo,Qiaosheng Pu Chem. Commun., 2019,55, 3963-3966
945217-56-1 (3-methyl-1H,4H,5H,6H-pyrrolo[3,4-c]pyrazole) Related Products
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