Product Name

  • Name

    S-CARBAMYL-L-CYSTEINE

  • EINECS 218-195-8
  • CAS No. 2072-71-1
  • Article Data2
  • CAS DataBase
  • Density 1.52 g/cm3
  • Solubility
  • Melting Point 164 °C (dec.)(lit.)
  • Formula C4H8N2O3S
  • Boiling Point 384.2°C at 760 mmHg
  • Molecular Weight 164.185
  • Flash Point 186.2°C
  • Transport Information
  • Appearance
  • Safety
  • Risk Codes
  • Molecular Structure Molecular Structure of 2072-71-1 (S-CARBAMYL-L-CYSTEINE)
  • Hazard Symbols
  • Synonyms Cysteine,carbamate (ester), L- (8CI);L-Cysteine, carbamate (ester) (9CI);Carbamicacid, thio-, S-ester with L-cysteine (8CI);3-Carbamylthioalanine;L-S-Carbamoylcysteine;NSC 102498;S-Carbamoyl-L-cysteine;S-Carbamoylcysteine;S-Carbamyl-L-cysteine;
  • PSA 131.71000
  • LogP 0.61080

L-Cysteine, S-(aminocarbonyl)- Specification

This chemical is called L-Cysteine, S-(aminocarbonyl)-, and it can also be named as Alanine, 3-thiocarbamoyl-, L-. With the molecular formula of C4H8N2O3S, its molecular weight is 164.18. The CAS registry number of this chemical is 2072-71-1. Additionally, its product category is Glycinescaffold.  

Other characteristics of the L-Cysteine, S-(aminocarbonyl)- can be summarised as followings: (1)ACD/LogP: -0.31; (2)# of Rule of 5 Violations: 1; (3)ACD/LogD (pH 5.5): -2.8; (4)ACD/LogD (pH 7.4): -2.91; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 1; (8)ACD/KOC (pH 7.4): 1; (9)#H bond acceptors: 5; (10)#H bond donors: 5; (11)#Freely Rotating Bonds: 5; (12)Polar Surface Area: 75.15 Å2; (13)Index of Refraction: 1.605; (14)Molar Refractivity: 37.2 cm3; (15)Molar Volume: 108 cm3; (16)Polarizability: 14.74×10-24cm3; (17)Surface Tension: 81.2 dyne/cm; (18)Density: 1.52 g/cm3; (19)Flash Point: 186.2 °C; (20)Enthalpy of Vaporization: 69.48 kJ/mol; (21)Boiling Point: 384.2 °C at 760 mmHg; (22)Vapour Pressure: 5.72E-07 mmHg at 25°C.

You can still convert the following datas into molecular structure: 
1.SMILES: O=C(O)[C@@H](N)CSC(=O)N
2.InChI: InChI=1/C4H8N2O3S/c5-2(3(7)8)1-10-4(6)9/h2H,1,5H2,(H2,6,9)(H,7,8)/t2-/m0/s1
3.InChIKey: YOAUVDYBDJTJJP-REOHCLBHBG

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intraperitoneal 1070mg/kg (1070mg/kg)   "Progress in Chemotherapy, Proceedings of the 8th International Congress on Chemotherapy, Athens, Greece, 1973," Daikos, G.K. ed., Athens, Greece, Hellenic Soc. for Chemotherapy, 1974Vol. 3, Pg. 771, 1974.
rat LD50 intraperitoneal 925mg/kg (925mg/kg)   "Progress in Chemotherapy, Proceedings of the 8th International Congress on Chemotherapy, Athens, Greece, 1973," Daikos, G.K. ed., Athens, Greece, Hellenic Soc. for Chemotherapy, 1974Vol. 3, Pg. 771, 1974.

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