18904-38-6 (N-benzylpyridine-2-carboxamide,N-benzylpyridine-2-carboxamide)

快速询单

结构式：

N-benzylpyridine-2-carboxamideMOL文件

CAS号：

18904-38-6

中文名称：

N-benzylpyridine-2-carboxamide

英文名称：

N-benzylpyridine-2-carboxamide

分子式：

C₁₃H₁₂N₂O

分子量：

212.247182846069

N-benzylpyridine-2-carboxamide(18904-38-6)名称与标识符

名称

中文别名：

N-benzylpyridine-2-carboxamide;

英文别名：

N-benzylpyridine-2-carboxamide;Benzyl 2-picolinamide;N-benzyl-2-pyridinecarboxamide;pyridine-2-carboxylic acid benzylamide;picolinic acid benzylamide;benzyl picolinamide;N-benzyl-2-pyridylcarboxamide;N-benzylpicolinamide;;HS-4328;2-Pyridinecarboxamide, N-(phenylmethyl)-;CBDivE_000043;CS-0362496;STK391105;DTXSID00350734;2-(N-benzylcarbamoyl)pyridine;starbld0037443;F70940;AKOS000629707;Z27749501;Oprea1_858379;Oprea1_054854;AB00073525-01;Cambridge id 5100084;18904-38-6;SCHEMBL3083971;N-Benzylpicolinamide;n-benzyl-2-pyridinecarboxamide;

标识符

InChIKey：

NNIFYECULHSHBH-UHFFFAOYSA-N

Inchi：

1S/C13H12N2O/c16-13(12-8-4-5-9-14-12)15-10-11-6-2-1-3-7-11/h1-9H,10H2,(H,15,16)

SMILES：

O=C(C1N=CC=CC=1)NCC1C=CC=CC=1

N-benzylpyridine-2-carboxamide(18904-38-6)物化性质

实验特性

LogP : 2.58640
PSA : 45.48000

计算特性

精确分子量 : 212.09500
氢键供体数量 : 1
氢键受体数量 : 2
可旋转化学键数量 : 3
同位素质量 : 212.094963011Da
重原子数量 : 16
复杂度 : 224
同位素原子数量 : 0
确定原子立构中心数量 : 0
不确定原子立构中心数量 : 0
确定化学键立构中心数量 : 0
不确定化学键立构中心数量 : 0
共价键单元数量 : 1
疏水参数计算参考值（XlogP） : 2
拓扑分子极性表面积 : 42Å²

N-benzylpyridine-2-carboxamide(18904-38-6)推荐厂家更多厂家(1)

公司名称	手机号/电话	联系人	QQ	微信	询单
上海吉至生化科技有限公司	18117592386 021-57481218	吉至试剂	3007522982		询单

N-benzylpyridine-2-carboxamide(18904-38-6)上下游

3-Phenylimidazo[1,5-a]pyridine

N-benzylpyridine-2-carboxamide(18904-38-6)相关文献

1. Synthesis of imides via palladium-catalyzed decarboxylative amidation of α-oxocarboxylic acids with secondary amides
Ning Xu,Jie Liu,Dengke Li,Lei Wang Org. Biomol. Chem. 2016 14 4749
2. RhI/RhIII catalyst-controlled divergent aryl/heteroaryl C–H bond functionalization of picolinamides with alkynes
ángel Manu Martínez,Javier Echavarren,Inés Alonso,Nuria Rodríguez,Ramón Gómez Arrayás,Juan C. Carretero Chem. Sci. 2015 6 5802
3. N-heterocyclic carbene-based ruthenium-catalyzed direct amidation of aldehydes with amines
Cheng Chen,Min Ha Kim,Soon Hyeok Hong Org. Chem. Front. 2015 2 241
4. Copper-catalyzed phosphorylation of sp2 C–H bonds
Shan Wang,Rui Guo,Gao Wang,Shan-Yong Chen,Xiao-Qi Yu Chem. Commun. 2014 50 12718
5. Merging cobalt and photoredox catalysis for the C8–H alkoxylation of 1-naphthylamine derivatives with alcohols
Zhaoliang Xu,Yu Hu,Lei Wang,Mingli Sun,Pinhua Li Org. Biomol. Chem. 2021 19 10112
6. Palladium-catalysed direct thiolation and selenation of aryl C–H bonds assisted by directing groups
Masayuki Iwasaki,Yasushi Nishihara Dalton Trans. 2016 45 15278
7. Recent developments in decarboxylative cross-coupling reactions between carboxylic acids and N–H compounds
Sattar Arshadi,Saeideh Ebrahimiasl,Akram Hosseinian,Aazam Monfared,Esmail Vessally RSC Adv. 2019 9 8964
8. 782. Pyrido[3,2-d]pyrimidin-4(3H)-ones
W. J. Irwin,D. G. Wibberley J. Chem. Soc. 1965 4240
9. Reactions of co-ordinated ligands. Part IV. The use of aminomagnesium compounds in the preparation of α-amino-acid amides from α-amino-acid ethyl esters
K. Bla?evi?,R. P. Houghton,C. S. Williams J. Chem. Soc. C 1968 1704
10. Studies on Wallach's imidazole synthesis
Tiziana Benincori,Elisabetta Brenna,Franco Sannicolo J. Chem. Soc. Perkin Trans. 1 1993 675

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960化工网为您提供N-benzylpyridine-2-carboxamide专业化合物百科信息，包括中文名，英文名，分子式，分子量，以及该化合物的CasNo.18904-38-6,相关理化性质;并提供了优质生产厂家信息包括厂家名称和联系方式等。 WAP版:18904-38-6 国际站:18904-38-6