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21149-17-7

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21149-17-7 Usage

Chemical Properties

White solid

Synthesis Reference(s)

Canadian Journal of Chemistry, 59, p. 406, 1981 DOI: 10.1139/v81-062The Journal of Organic Chemistry, 31, p. 3928, 1966Synthetic Communications, 19, p. 695, 1989 DOI: 10.1080/00397918908050717

Check Digit Verification of cas no

The CAS Registry Mumber 21149-17-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,1,4 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 21149-17:
(7*2)+(6*1)+(5*1)+(4*4)+(3*9)+(2*1)+(1*7)=77
77 % 10 = 7
So 21149-17-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H13NO4/c1-9(11(14)16-2)13-12(15)17-8-10-6-4-3-5-7-10/h3-7H,1,8H2,2H3,(H,13,15)

21149-17-7 Well-known Company Product Price

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  • Aldrich

  • (96077)  Z-Dehydro-Ala-OMe  ≥98.0% (TLC)

  • 21149-17-7

  • 96077-1G

  • 2,094.30CNY

  • Detail

21149-17-7SDS

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 methyl 2-(phenylmethoxycarbonylamino)prop-2-enoate

1.2 Other means of identification

Product number -
Other names Z-Dehydroalanine methyl ester

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:21149-17-7 SDS

21149-17-7Relevant articles and documents

Wojciechowska et al.

, p. 4063 (1978)

3-Imidoallenylphosphonates: In Situ Formation and β-Alkoxylation

Berton, Jan K. E. T.,Heugebaert, Thomas S. A.,Debrouwer, Wouter,Stevens, Christian V.

, p. 208 - 211 (2016)

3-Imidoallenylphosphonates, allenes bearing both an electron-withdrawing and -donating group, were isolated for the first time. An alkoxy substituent was introduced into these unprecedented intermediates in a one-pot approach, yielding β-functionalized am

Conjugate addition of ammo acid side chains to alkynones and alkynoic acid derivatives

Crisp, Geoffrey T.,Millan, Michael J.

, p. 637 - 648 (1998)

Suitably protected amino acids were used to investigate the Michael addition of the sulfanyl group of cysteine, the hydroxyl group of serine and the ε-amino group of lysine to a conjugated alkynone, alkynoic ester and alkynoic amide. The expected heterosu

SULFUR EXTRUSION FROM DISULFIDES BY CARBENES

-

Page/Page column 30; 39-42, (2021/10/30)

The present invention relates to a method for preparing a compound T having a thioether group from a compound D having a disulfide group in the presence of a carbene.

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