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117490-34-3

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117490-34-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117490-34-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,4,9 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 117490-34:
(8*1)+(7*1)+(6*7)+(5*4)+(4*9)+(3*0)+(2*3)+(1*4)=123
123 % 10 = 3
So 117490-34-3 is a valid CAS Registry Number.

117490-34-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(3-indolylmethylene)hydantoin

1.2 Other means of identification

Product number -
Other names 5-[(1H-indol-3-yl)methylidene]imidazolidine-2,4-dione

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:117490-34-3 SDS

117490-34-3Relevant articles and documents

Iminophosphorane-Mediated Imidazole Ring Formation: A New and General Entry to Aplysinopsin-type Alkaloids of Marine Origin

Molina, Pedro,Almendros, Pedro,Fresneda, Pilar M.

, p. 2241 - 2254 (1994)

Aza Wittig-type reactions of iminophosphoranes 21, derived from ethyl α-azido-β-(3-indolyl)propenoates and triphenylphosphine, with methyl isocyanate, carbon dioxide or carbon disulfide provide the corresponding heterocumulenes 22, 25 and 28 which undergo

-

Shabica et al.

, p. 1156 (1946)

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Hydantoin-based molecular photoswitches

Martínez-López, David,Yu, Meng-Long,García-Iriepa, Cristina,Campos, Pedro J.,Frutos, Luis Manuel,Golen, James A.,Rasapalli, Sivappa,Sampedro, Diego

, p. 3929 - 3939 (2015/05/05)

A new family of molecular photoswitches based on arylidenehydantoins is described together with their synthesis and photochemical and photophysical studies. A series of hydantoin derivatives have been prepared as single isomers using simple and versatile chemistry in good yields. Our studies show that the photostationary states of these compounds can be easily controlled by means of external factors, such as the light source or filters. Moreover, the detailed investigations proved that these switches are efficient (i.e., they make efficient use of the light energy, are high fatigue resistant, and are very photostable). In some cases, the switches can be completely turned on/off, a desirable feature for specific applications. A series of theoretical calculations have also been carried out to understand the photoisomerization mechanism at the molecular level.

Anticonvulsant Activity of Phenylmethylenehydantoins: A Structure-Activity Relationship Study

Thenmozhiyal, Jeyanthi Chinnappa,Wong, Peter Tsun-Hon,Chui, Wai-Keung

, p. 1527 - 1535 (2007/10/03)

Phenylmethylenehydantoins (PMHs) and their des-phenyl analogues were synthesized and evaluated for anticonvulsant activity using the maximal electroshock seizure (MES) assay. The phenyl rings of PMHs were substituted with a wide spectrum of groups, and th

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