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73870-54-9

phenylmethyl [3,3-bis(ethyloxy)propyl]carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 73870-54-9 Structure

  • Basic information

    1. Product Name: phenylmethyl [3,3-bis(ethyloxy)propyl]carbamate
    2. Synonyms: phenylmethyl [3,3-bis(ethyloxy)propyl]carbamate
    3. CAS NO:73870-54-9
    4. Molecular Formula:
    5. Molecular Weight: 281.352
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 73870-54-9.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: phenylmethyl [3,3-bis(ethyloxy)propyl]carbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: phenylmethyl [3,3-bis(ethyloxy)propyl]carbamate(73870-54-9)
    11. EPA Substance Registry System: phenylmethyl [3,3-bis(ethyloxy)propyl]carbamate(73870-54-9)

  • 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: 73870-54-9(Hazardous Substances Data)

73870-54-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73870-54-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,8,7 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 73870-54:
(7*7)+(6*3)+(5*8)+(4*7)+(3*0)+(2*5)+(1*4)=149
149 % 10 = 9
So 73870-54-9 is a valid CAS Registry Number.

73870-54-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(benzyloxycarbonylamino)propionaldehyde diethyl acetal

1.2 Other means of identification

Product number -
Other names -

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:73870-54-9 SDS

73870-54-9Relevant articles and documents

Enantioselective organo-SOMO cycloadditions: A catalytic approach to complex pyrrolidines from olefins and aldehydes

Jui, Nathan T.,Garber, Jeffrey A.O.,Finelli, Fernanda Gadini,MacMillan, David W.C.

supporting information; experimental part, p. 11400 - 11403 (2012/09/05)

A new method to rapidly generate pyrrolidines via a SOMO-activated enantioselective (3 + 2) coupling of aldehydes and conjugated olefins has been accomplished. A radical-polar crossover mechanism is proposed wherein olefin addition to a transient enamine

Synthesis of L-Epicapreomycidine

Teshima, Tadashi,Konishi, Kunikazu,Shiba, Tetsuo

, p. 508 - 511 (2007/10/02)

A cyclic guanidino amino acid, L-epicapreomycidine, isolated from hydrolyzates of protease inhibitors such as chymostatin and elastatinal was synthetised.This amino acid is as diastereomer of L-capreomycidine which is a component amino acid of tuberactino

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