Question 1

秀谷隆 的 CAS 号是多少？

Accepted Answer

秀谷隆 的 CAS 登记号为 3060-89-7。

Question 2

秀谷隆 的分子式与分子量是多少？

Accepted Answer

分子式 C9H11BrN2O2，分子量 259.10。

Question 3

秀谷隆 还有哪些别名？

Accepted Answer

别名/同义词：秀谷隆、Metobromuron。

Question 4

秀谷隆 的登记用途是什么？

Accepted Answer

登记用途：Uses: Used as pre-emergence herbicide to control annual broad-leaved weeds and grasses in beans、soybeans、tomatoes、tobacco、potatoes、flax、and sunflowers、Not sold in the US、[HSDB] Used in the EU as herbicide on potatoes、[ExPub: EC: EFSA]、Farming (Pesticides) [Category: Industry]、Used on beans、and sunflowers.、IT IS A、SELECTIVE PRE-EMERGENT ANNUAL BROADLEAFED WEED AND GRASS CONTROL IN POTATOES、WHITE (FIELD) AND SNAP (BUSH) BEANS、AT 1.5-2.5 KG AI、HECTARE ...、IT IS、SOMEWHAT LESS EFFECTIVE AGAINST GRASSES、PARTICULARLY AT LOW RATES.、... RECOMMENDED FOR PRE-EMERGENCE USE ON POTATOES、BEANS、GROUNDNUTS AT RATES OF 1.5-2.0 KG AI、HECTARE、ON TOBACCO PRIOR TO TRANSPLANTING AT 1.5-2.5 KG AI、HECTARE.、As a herbicide.、Use Classification: Environmental transformation -> Pesticides (parent、predecessor)、Herbicides、Methods of Manufacturing: PREPARED BY BROMINATION OF N-PHENYL-N'-METHOXY-N'-METHYLUREA: H MARTIN ET AL、SWISS PATENT 405、821 CORRESP TO US PATENT 3、288、851 (BOTH 1966 TO CIBA).、BY BROMINATION OF 1-METHOXY-1-METHYL-3-PHENYLUREA OR BY REACTION OF 4-BROMOPHENYL ISOCYANATE WITH O、N-DIMETHYLHYDROXYLAMINE. ... BRITISH PATENT 965、313、US PATENT 3、223、721.、Reaction of p-bromoaniline with phosgene and N、O-dimethylhydroxylamine (phosgenation、isocyanate addition).、Formulations、Preparations: 50% wettable powder (BASF、Ciba-Geigy). In combination with metolachlor (Galex and Tobacron) or with terbutryn (Ingrater) Ciba-Geigy、4 lb、gal (400 g、l) flowable (BASF)、Combinations: Igrater 50 WP (metobromuron 25% and terbutryn 25%)、Galex 500 EC (metobromuron + metolachlor 1:1 or 2:3)、C 3126、Ciba-3126、For more Formulations、Preparations (Complete) data for METOBROMURON (6 total)、please visit the HSDB record page.、General Manufacturing Information: Metobromuron is the bromophenyl analog of monuron.、Not marketed in USA.、...、IT、BECOMES NON-PHYTOTOXIC IN 3 MO AT RECOMMENDED DOSAGES.、Substituted ureas may be hydrolyzed、whereby the end products are carbon dioxide and the corresponding amines. Hydrolysis proceeds under acid as well as alkaline conditions. This reaction is used for the quantitative analysis of active ingredients and、or residues of urea herbicide preparations by determining either the aromatic or the aliphatic amine moiety.。

CAS 号	3060-89-7
PubChem CID	18290
分子式	C9H11BrN2O2
IUPAC 名称	3-(4-bromophenyl)-1-methoxy-1-methylurea
UNII（FDA）	4251089P3L

Molecular Weight	259.10
XLogP3	2.4
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	2
Exact Mass	258.00039
Monoisotopic Mass	258.00039
Topological Polar Surface Area	41.6
Heavy Atom Count	14

Melting Point	95-96 °C
Vapor Pressure	0.000003 [mmHg]
Vapor Pressure	3X10-6 MM HG @ 20 °C
LogP	2.41
Formulations/Preparations	C 3126
Formulations/Preparations	Ciba-3126

GHS 通报统计	5.1% (3 / 59)
已通报的危害声明	H302 (93.2%), H332 (93.2%), H351 (27.1%), H373 (28.8%), H400 (27.1%), H410 (28.8%)

秀谷隆

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CAS号	3060-89-7
分子式	C9H11BrN2O2
分子量	259.10
熔点	95-96 °C
LogP	2.41
应用领域	Uses: Used as pre-emergence herbicide to control annual broad-leaved weeds and grasses in beans、soybeans、tomatoes、tobacco、potatoes、flax、and sunflowers、Not sold in the US、[HSDB] Used in the EU as herbicide on potatoes、[ExPub: EC: EFSA]、Farming (Pesticides) [Category: Industry]、Used on beans、and sunflowers.、IT IS A、SELECTIVE PRE-EMERGENT ANNUAL BROADLEAFED WEED AND GRASS CONTROL IN POTATOES、WHITE (FIELD) AND SNAP (BUSH) BEANS、AT 1.5-2.5 KG AI、HECTARE ...、IT IS、SOMEWHAT LESS EFFECTIVE AGAINST GRASSES、PARTICULARLY AT LOW RATES.、... RECOMMENDED FOR PRE-EMERGENCE USE ON POTATOES、BEANS、GROUNDNUTS AT RATES OF 1.5-2.0 KG AI、HECTARE、ON TOBACCO PRIOR TO TRANSPLANTING AT 1.5-2.5 KG AI、HECTARE.、As a herbicide.、Use Classification: Environmental transformation -> Pesticides (parent、predecessor)、Herbicides、Methods of Manufacturing: PREPARED BY BROMINATION OF N-PHENYL-N'-METHOXY-N'-METHYLUREA: H MARTIN ET AL、SWISS PATENT 405、821 CORRESP TO US PATENT 3、288、851 (BOTH 1966 TO CIBA).、BY BROMINATION OF 1-METHOXY-1-METHYL-3-PHENYLUREA OR BY REACTION OF 4-BROMOPHENYL ISOCYANATE WITH O、N-DIMETHYLHYDROXYLAMINE. ... BRITISH PATENT 965、313、US PATENT 3、223、721.、Reaction of p-bromoaniline with phosgene and N、O-dimethylhydroxylamine (phosgenation、isocyanate addition).、Formulations、Preparations: 50% wettable powder (BASF、Ciba-Geigy). In combination with metolachlor (Galex and Tobacron) or with terbutryn (Ingrater) Ciba-Geigy、4 lb、gal (400 g、l) flowable (BASF)、Combinations: Igrater 50 WP (metobromuron 25% and terbutryn 25%)、Galex 500 EC (metobromuron + metolachlor 1:1 or 2:3)、C 3126、Ciba-3126、For more Formulations、Preparations (Complete) data for METOBROMURON (6 total)、please visit the HSDB record page.、General Manufacturing Information: Metobromuron is the bromophenyl analog of monuron.、Not marketed in USA.、...、IT、BECOMES NON-PHYTOTOXIC IN 3 MO AT RECOMMENDED DOSAGES.、Substituted ureas may be hydrolyzed、whereby the end products are carbon dioxide and the corresponding amines. Hydrolysis proceeds under acid as well as alkaline conditions. This reaction is used for the quantitative analysis of active ingredients and、or residues of urea herbicide preparations by determining either the aromatic or the aliphatic amine moiety.