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21076-38-0

Hydrazinecarbothioamide, 2-(1-methylethyl)-N-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 21076-38-0 Structure

  • Basic information

    1. Product Name: Hydrazinecarbothioamide, 2-(1-methylethyl)-N-phenyl-
    2. Synonyms:
    3. CAS NO:21076-38-0
    4. Molecular Formula: C10H15N3S
    5. Molecular Weight: 209.315
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 21076-38-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Hydrazinecarbothioamide, 2-(1-methylethyl)-N-phenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Hydrazinecarbothioamide, 2-(1-methylethyl)-N-phenyl-(21076-38-0)
    11. EPA Substance Registry System: Hydrazinecarbothioamide, 2-(1-methylethyl)-N-phenyl-(21076-38-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 21076-38-0(Hazardous Substances Data)

21076-38-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21076-38-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,0,7 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21076-38:
(7*2)+(6*1)+(5*0)+(4*7)+(3*6)+(2*3)+(1*8)=80
80 % 10 = 0
So 21076-38-0 is a valid CAS Registry Number.

21076-38-0SDS

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 1-phenyl-3-(propan-2-ylamino)thiourea

1.2 Other means of identification

Product number -
Other names 1-Isopropyl-4-phenyl-thiosemicarbazid

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:21076-38-0 SDS

21076-38-0Downstream Products

21076-38-0Relevant articles and documents

Restricted Rotation around the N-N Bond in 4-Phenylsemicarbazides and Thiosemicarbazides

Blandov,Gindin,Kuznetsov

, p. 1417 - 1423 (2007/10/03)

Reaction of 1,1-dialkylhydrazines with phenylisocyanate or phenylisothiocyanate yields stereo-specifically to the (EZ)-isomers of the corresponding 1,1-dialkyl-4-phenyl(thio)semicarbazides R1R2NNHC(=Z)NHPh (Z = O, S). In the NMR spec

Synthesis and Some Reactions of 2-Imino-2,5-dihydro-1,3,4-thiadiazoles. Formation of β-Lactams

Yamamoto, Iwao,Abe, Ikuo,Nozawa, Muneharu,Kotani, Mitsuhiro,Motoyoshiya, Jiro,et al.

, p. 2297 - 2301 (2007/10/02)

The title compounds, 2-imino-2,5-dihydro-1,3,4-thiadiazoles (2a-c), were prepared by oxidation of thiosemicarbazones.The reactions of (2a-c) with ketenes gave the spiro-β-lactams (7a-d), via cycloaddition.On the other hand, the reaction of (2a) with phenyl isocyanate gave the thiohydantoins (9) and (10).The reactions of compound (2) with some other nucleophiles are also described.

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