AG22070

503555-50-8 | 6-Chloro-4-methylpyridine-3-carboxylic acid

Manufacturer: A2B Chem

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CatalogNumber

AG22070

ChemicalName

6-Chloro-4-methylpyridine-3-carboxylic acid

CasNumber

503555-50-8

MolecularFormula

C7H6ClNO2

MolecularWeight

171.581

MdlNumber

MFCD12755871

Smiles

Cc1cc(Cl)ncc1C(=O)O

Complexity

163

Covalently-bondedUnitCount

1

HeavyAtomCount

11

HydrogenBondAcceptorCount

3

HydrogenBondDonorCount

1

RotatableBondCount

1

Xlogp3

1.7

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Compare Similar Items

Show Difference

Img

A2B Chem

AG22070

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CatalogNumber:
AG22070

ChemicalName:
6-Chloro-4-methylpyridine-3-carboxylic acid

CasNumber:
503555-50-8

MolecularFormula:
C7H6ClNO2

MolecularWeight:
171.581

MdlNumber:
MFCD12755871

Smiles:
Cc1cc(Cl)ncc1C(=O)O

Complexity:
163

Covalently-bondedUnitCount:
1

HeavyAtomCount:
11

HydrogenBondAcceptorCount:
3

HydrogenBondDonorCount:
1

RotatableBondCount:
1

Xlogp3:
1.7

Img

A2B Chem

AG22071

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CatalogNumber:
AG22071

ChemicalName:
5-(Bromomethyl)-1H-indazole

CasNumber:
496842-04-7

MolecularFormula:
C8H7BrN2

MolecularWeight:
211.05857999999998

MdlNumber:
MFCD09475772

Smiles:
BrCc1ccc2c(c1)cn[nH]2

Complexity:
__

Covalently-bondedUnitCount:
__

HeavyAtomCount:
__

HydrogenBondAcceptorCount:
__

HydrogenBondDonorCount:
__

RotatableBondCount:
__

Xlogp3:
__

Img

A2B Chem

AG22072

--


CatalogNumber:
__

ChemicalName:
__

CasNumber:
__

MolecularFormula:
__

MolecularWeight:
__

MdlNumber:
__

Smiles:
Cc1cnc(c(c1)C)C(=O)O

Complexity:
__

Covalently-bondedUnitCount:
__

HeavyAtomCount:
__

HydrogenBondAcceptorCount:
__

HydrogenBondDonorCount:
__

RotatableBondCount:
__

Xlogp3:
__

Img

A2B Chem

AG22073

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CatalogNumber:
AG22073

ChemicalName:
4-(2-Bromo-4-nitrophenyl)morpholine

CasNumber:
477846-96-1

MolecularFormula:
C10H11BrN2O3

MolecularWeight:
287.10994

MdlNumber:
MFCD02081938

Smiles:
Brc1cc(ccc1N1CCOCC1)[N+](=O)[O-]

Complexity:
253

Covalently-bondedUnitCount:
1

HeavyAtomCount:
16

HydrogenBondAcceptorCount:
4

HydrogenBondDonorCount:
__

RotatableBondCount:
1

Xlogp3:
2.2