Scholarly article on Methyl-carbamic acid 3-(3-hydroxy-1-methyl-propyl)-phenyl ester 51038-72-3 from Journal of Agricultural and Food Chemistry p. 1037,1042

DOI: 10.1021/jf60190a046

Source and publish data:

Journal of Agricultural and Food Chemistry p. 1037,1042 (1973)

Update date:2022-08-03

Topics:

Authors:

Cheng Cheng

Casida Casida

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1021/jf60190a046

Full text of DOI:10.1021/jf60190a046

Products guided by the article

Product name:Methyl-carbamic acid 3-(3-hydroxy-1-methyl-propyl)-phenyl ester

Cas No:51038-72-3

R&D Labs maybe for 51038-72-3

Longhui qunfeng Chemical Co., Ltd

Contact:86-731-82173407

Address:South-east Industrial Park, Longhui County, Hunan Province, China
CHEMINN LTD.

website:http://www.cheminn.com/

Contact:86-531-67875205

Address:No.9-2,South of Shanda Road, Jinan ,China
CHENGDU CHENLV HERB CO.,LTD

Contact:+86-28-88523492

Address:714rooms of Time Square, Pujiang County
Zhejiang Newfine Industry Co.,Ltd.

Contact:+86-573-82262042

Address:No.225,Dongqing Road, garoms@163.com
Jinhua City Mingzhu Pharmaceutical Co.,Ltd.

Contact:15857995878 0579-82207761

Address:No.169 Shenze Road, New Area,Jinpan Development Zone, Jinhua

Relevant to this article

Large-scale synthesis of "Cpep" RNA monomers and their application in automated RNA synthesis

Doi:10.1081/NCN-200060150
(2005)
THE PHOTOCHEMISTRY OF AZO DYES. PHOTOISOMERISATION VERSUS PHOTOREDUCTION FROM 4-DIETHYLAMINOAZOBENZENE AND 4-DIETHYLAMINO-4'-METHOXYAZOBENZENE.

Doi:10.1039/P29830001021
(1983)
Aza-Payne rearrangement of α,α-disubstituted-aziridinemethanols

Doi:10.1016/j.tetasy.2006.04.035
(2006)
Doi:10.1039/jr9580000379
(1958)
Triterpene glycosides from Tragacantha stipulosa and their genins. Structure of cyclostipuloside E

Doi:10.1023/B:CONC.0000025463.46079.8f
(2004)
Synthesis and antitumor activity of two natural N-acetylglucosamine-bearing triterpenoid saponins: Lotoidoside D and E

Doi:10.1016/j.bmcl.2006.05.086
(2006)

Article Doi

DOI: 10.1021/jf60190a046